Canonical Allele Identifier: CA115200
Gene: CYP17A1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1802
ClinVar RCV Id: RCV000001875
dbSNP Id: rs104894153

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837075C>T , CM000672.2:g.102837075C>T GRCh38
NC_000010.10:g.104596832C>T , CM000672.1:g.104596832C>T GRCh37
NC_000010.9:g.104586822C>T NCBI36
NG_007955.1:g.5459G>A

Transcript Alleles

HGVS Amino-acid change
NM_000102.3:c.287G>A VV NP_000093.1:p.Arg96Gln
NM_000102.4:c.287G>A VV MANE Preferred NP_000093.1:p.Arg96Gln
ENST00000369887.3:c.287G>A ENSP00000358903.3:p.Arg96Gln
ENST00000489268.1:n.340G>A