Product Details

Primer Sequences
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Primer Chromosome Location
Chr.X: 110202361-110202632 on Build GRCh38
Format
Each primer will be delivered in a single tube, dried-down
Quick Reference Guide
Primer Designer™ Tool Quick Reference
Ampliseq ID's

Gene Details

Gene Symbol
AMMECR1
Entrez Gene ID
9949
Gene Name
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Gene Aliases
AMMERC1
UniGene
Hs.656243
Gene Chromosome Location
Chr.X: 110194186-110440233 on Build GRCh38
Transcripts
NM_001025580.1 NM_001171689.1 NM_015365.2

SNP Detail

SNP ID Chromosome Location
rs768604692 Chr.X: 110202536-110202536 on Build GRCh38
rs754001465 Chr.X: 110202435-110202437 on Build GRCh38
rs779348289 Chr.X: 110202420-110202420 on Build GRCh38
rs765510526 Chr.X: 110202564-110202565 on Build GRCh38
rs759367448 Chr.X: 110202436-110202436 on Build GRCh38
rs985011367 Chr.X: 110202576-110202576 on Build GRCh38
rs958661940 Chr.X: 110202462-110202462 on Build GRCh38
rs867942217 Chr.X: 110202517-110202517 on Build GRCh38
rs974317684 Chr.X: 110202484-110202484 on Build GRCh38
rs930165816 Chr.X: 110202507-110202507 on Build GRCh38
rs140856361 Chr.X: 110202486-110202486 on Build GRCh38
rs747190504 Chr.X: 110202471-110202471 on Build GRCh38
rs774399743 Chr.X: 110202564-110202564 on Build GRCh38
rs759627261 Chr.X: 110202547-110202548 on Build GRCh38
rs752938961 Chr.X: 110202586-110202590 on Build GRCh38
rs748689723 Chr.X: 110202421-110202421 on Build GRCh38
rs758447381 Chr.X: 110202424-110202424 on Build GRCh38
rs777963039 Chr.X: 110202465-110202465 on Build GRCh38
rs765240698 Chr.X: 110202577-110202577 on Build GRCh38
rs866602703 Chr.X: 110202466-110202466 on Build GRCh38
rs868514440 Chr.X: 110202467-110202467 on Build GRCh38
rs771116750 Chr.X: 110202477-110202477 on Build GRCh38
rs747363061 Chr.X: 110202515-110202515 on Build GRCh38

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