Canonical Allele Identifier: CA212296494
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs947279085
gnomAD v3: 10-102837486-G-T
gnomAD v4: 10-102837486-G-T
MyVariant Identifiers: chr10:g.104597243G>T (hg19) chr10:g.102837486G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837486G>T , CM000672.2:g.102837486G>T GRCh38
NC_000010.10:g.104597243G>T , CM000672.1:g.104597243G>T GRCh37
NC_000010.9:g.104587233G>T NCBI36
NG_007955.1:g.5048C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-125C>A ENSP00000358903.3:n.-125C>A
NM_000102.3:c.-125C>A NP_000093.1:n.-125C>A
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