Canonical Allele Identifier: CA212296456

Gene: CYP17A1

Linked Data

• dbSNP Id: rs61754260
• gnomAD v3: 10-102837437-C-T
• gnomAD v4: 10-102837437-C-T
• MyVariant Identifiers: chr10:g.104597194C>T (hg19) ; chr10:g.102837437C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837437C>T , CM000672.2:g.102837437C>T	GRCh38
NC_000010.10:g.104597194C>T , CM000672.1:g.104597194C>T	GRCh37
NC_000010.9:g.104587184C>T	NCBI36
NG_007955.1:g.5097G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638190.1:c.-76G>A	ENSP00000492539.1:n.-76G>A
ENST00000638971.1:c.-76G>A	ENSP00000492313.1:n.-76G>A
ENST00000369887.3:c.-76G>A	ENSP00000358903.3:n.-76G>A
NM_000102.3:c.-76G>A	NP_000093.1:n.-76G>A