Canonical Allele Identifier: CA659061717

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1377450605
• gnomAD v3: 10-102837512-C-T
• gnomAD v4: 10-102837512-C-T
• MyVariant Identifiers: chr10:g.104597269C>T (hg19) ; chr10:g.102837512C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837512C>T , CM000672.2:g.102837512C>T	GRCh38
NC_000010.10:g.104597269C>T , CM000672.1:g.104597269C>T	GRCh37
NC_000010.9:g.104587259C>T	NCBI36
NG_007955.1:g.5022G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.3:c.-151G>A	ENSP00000358903.3:n.-151G>A
NM_000102.3:c.-151G>A	NP_000093.1:n.-151G>A