Canonical Allele Identifier: CA120695
Gene: AR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9810
ClinVar RCV Id: RCV000010484
dbSNP Id: rs137852567

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67717595A>G , CM000685.2:g.67717595A>G GRCh38
NC_000023.10:g.66937437A>G , CM000685.1:g.66937437A>G GRCh37
NC_000023.9:g.66854162A>G NCBI36
NG_009014.2:g.178564A>G

Transcript Alleles

HGVS Amino-acid change
NM_000044.3:c.2291A>G VV NP_000035.2:p.Tyr764Cys
NM_001011645.2:c.695A>G VV NP_001011645.1:p.Tyr232Cys
NM_000044.4:c.2291A>G VV NP_000035.2:p.Tyr764Cys
NM_001011645.3:c.695A>G VV NP_001011645.1:p.Tyr232Cys
ENST00000374690.7:c.2291A>G ENSP00000363822.3:p.Tyr764Cys
ENST00000396043.2:c.695A>G ENSP00000379358.2:p.Tyr232Cys
ENST00000396044.7:c.2173+5906A>G ENSP00000379359.3:p.=
ENST00000612452.4:c.1721A>G ENSP00000484033.1:p.Tyr574Cys