Canonical Allele Identifier: CA10630845

Gene: CYP17A1

Linked Data

• ClinVar Variation Id: 298631
• ClinVar RCV Id: RCV000259333
• dbSNP Id: rs58519757
• gnomAD v2: 10-104597284-C-G
• gnomAD v3: 10-102837527-C-G
• gnomAD v4: 10-102837527-C-G
• MyVariant Identifiers: chr10:g.104597284C>G (hg19) ; chr10:g.102837527C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837527C>G , CM000672.2:g.102837527C>G	GRCh38
NC_000010.10:g.104597284C>G , CM000672.1:g.104597284C>G	GRCh37
NC_000010.9:g.104587274C>G	NCBI36
NG_007955.1:g.5007G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.3:c.-166G>C	ENSP00000358903.3:n.-166G>C
NM_000102.3:c.-166G>C	NP_000093.1:n.-166G>C