Canonical Allele Identifier: CA115188
Gene: CYP17A1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1791
ClinVar RCV Id: RCV000001864
dbSNP Id: rs104894146

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837084A>C , CM000672.2:g.102837084A>C GRCh38
NC_000010.10:g.104596841A>C , CM000672.1:g.104596841A>C GRCh37
NC_000010.9:g.104586831A>C NCBI36
NG_007955.1:g.5450T>G

Transcript Alleles

HGVS Amino-acid change
NM_000102.3:c.278T>G VV NP_000093.1:p.Phe93Cys
NM_000102.4:c.278T>G VV MANE Preferred NP_000093.1:p.Phe93Cys
ENST00000369887.3:c.278T>G ENSP00000358903.3:p.Phe93Cys
ENST00000489268.1:n.331T>G