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TGCAAAACCTGTGTGTGTATCTATA[C/T]ACTTACCTTTTGTGTTAAGAAAGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 107910 MIM: 608603 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP19A1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CYP19A1 - cytochrome P450 family 19 subfamily A member 1 | ||||||
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There are no transcripts associated with this gene. |
GLDN - gliomedin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_181789.2 | Intron | NP_861454.2 | ||||
XM_011521501.2 | Intron | XP_011519803.1 | ||||
XM_017022121.1 | Intron | XP_016877610.1 | ||||
XM_017022122.1 | Intron | XP_016877611.1 | ||||
XM_017022123.1 | Intron | XP_016877612.1 | ||||
XM_017022124.1 | Intron | XP_016877613.1 | ||||
XM_017022125.1 | Intron | XP_016877614.1 | ||||
XM_017022126.1 | Intron | XP_016877615.1 |