Canonical Allele Identifier: CA115179
Gene: CYP17A1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1780
dbSNP Id: rs104894135

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835374A>G , CM000672.2:g.102835374A>G GRCh38
NC_000010.10:g.104595131A>G , CM000672.1:g.104595131A>G GRCh37
NC_000010.9:g.104585121A>G NCBI36
NG_007955.1:g.7160T>C

Transcript Alleles

HGVS Amino-acid change
NM_000102.3:c.316T>C VV NP_000093.1:p.Ser106Pro
NM_000102.4:c.316T>C VV MANE Preferred
ENST00000369887.3:c.316T>C ENSP00000358903.3:p.Ser106Pro
ENST00000489268.1:n.570T>C