Canonical Allele Identifier: CA115198
Gene: CYP17A1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1801
ClinVar RCV Id: RCV000001874
dbSNP Id: rs104894152
MyVariant Identifiers: chr10:g.104597038G>T (hg19) chr10:g.102837281G>T (hg38)

User contributed link-outs

PubMed: PMID:15811924
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837281G>T , CM000672.2:g.102837281G>T GRCh38
NC_000010.10:g.104597038G>T , CM000672.1:g.104597038G>T GRCh37
NC_000010.9:g.104587028G>T NCBI36
NG_007955.1:g.5253C>A

Transcript Alleles

HGVS Amino-acid change
NM_000102.3:c.81C>A VV NP_000093.1:p.Tyr27Ter
NM_000102.4:c.81C>A VV MANE Preferred
ENST00000369887.3:c.81C>A ENSP00000358903.3:p.Tyr27Ter
ENST00000489268.1:n.134C>A
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