Canonical Allele Identifier: CA115198

Gene: CYP17A1

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)
• PubMed: PMID:15811924

User contributed link-outs

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	NP_000093.1:p.Tyr27Ter
ENST00000369887.3:c.81C>A	ENSP00000358903.3:p.Tyr27Ter
ENST00000489268.1:n.134C>A