Product Details

SNP ID
rs17047134
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:25740488 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTCCAAATTAGGAGACTTGAAATCA[A/G]TATGCAAATGATGCAAATTGACACT
Phenotype
MIM: 612991
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ASXL2 PubMed Links

Gene Details

Gene
ASXL2
Gene Name
additional sex combs like 2, transcriptional regulator
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018263.4 5477 UTR 3 NP_060733.4
XM_006712039.3 5477 UTR 3 XP_006712102.1
XM_006712040.2 5477 UTR 3 XP_006712103.1
XM_011532950.2 5477 UTR 3 XP_011531252.1
XM_011532951.2 5477 UTR 3 XP_011531253.1
XM_017004429.1 5477 UTR 3 XP_016859918.1
XM_017004430.1 5477 UTR 3 XP_016859919.1

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