Canonical Allele Identifier: CA5669536
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2829700
ClinVar RCV Id: RCV003686399
dbSNP Id: rs148082634
ExAC: 10:104594680 G / C
gnomAD v2: 10-104594680-G-C
gnomAD v3: 10-102834923-G-C
gnomAD v4: 10-102834923-G-C
MyVariant Identifiers: chr10:g.104594680G>C (hg19) chr10:g.102834923G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834923G>C , CM000672.2:g.102834923G>C GRCh38
NC_000010.10:g.104594680G>C , CM000672.1:g.104594680G>C GRCh37
NC_000010.9:g.104584670G>C NCBI36
NG_007955.1:g.7611C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.528C>G MANE Select ENSP00000358903.3:p.Thr176=
ENST00000638190.1:c.528C>G ENSP00000492539.1:p.Thr176=
ENST00000638272.1:c.298-1715C>G ENSP00000491508.1:n.298-1715C>G
ENST00000638971.1:c.528C>G ENSP00000492313.1:p.Thr176=
ENST00000639393.1:c.528C>G ENSP00000492651.1:p.Thr176=
ENST00000640633.1:n.290C>G
ENST00000369887.3:c.528C>G ENSP00000358903.3:p.Thr176=
ENST00000489268.1:n.782C>G
NM_000102.3:c.528C>G NP_000093.1:p.Thr176=
NM_000102.4:c.528C>G MANE Select NP_000093.1:p.Thr176=
Search 100 bp 5'
Search 100 bp 3'