Canonical Allele Identifier: CA659061719

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1199970718
• gnomAD v3: 10-102837520-G-T
• gnomAD v4: 10-102837520-G-T
• MyVariant Identifiers: chr10:g.104597277G>T (hg19) ; chr10:g.102837520G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837520G>T , CM000672.2:g.102837520G>T	GRCh38
NC_000010.10:g.104597277G>T , CM000672.1:g.104597277G>T	GRCh37
NC_000010.9:g.104587267G>T	NCBI36
NG_007955.1:g.5014C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.3:c.-159C>A	ENSP00000358903.3:n.-159C>A
NM_000102.3:c.-159C>A	NP_000093.1:n.-159C>A