Canonical Allele Identifier: CA120752
Gene: AR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9836
ClinVar RCV Id: RCV000010510
dbSNP Id: rs137852583

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67711680G>A , CM000685.2:g.67711680G>A GRCh38
NC_000023.10:g.66931522G>A , CM000685.1:g.66931522G>A GRCh37
NC_000023.9:g.66848247G>A NCBI36
NG_009014.2:g.172649G>A

Transcript Alleles

HGVS Amino-acid change
NM_000044.3:c.2164G>A VV NP_000035.2:p.Ala722Thr
NM_001011645.2:c.568G>A VV NP_001011645.1:p.Ala190Thr
NM_000044.4:c.2164G>A VV NP_000035.2:p.Ala722Thr
NM_001011645.3:c.568G>A VV NP_001011645.1:p.Ala190Thr
ENST00000374690.7:c.2164G>A ENSP00000363822.3:p.Ala722Thr
ENST00000396043.2:c.568G>A ENSP00000379358.2:p.Ala190Thr
ENST00000396044.7:c.2164G>A ENSP00000379359.3:p.Ala722Thr
ENST00000612452.4:c.1594G>A ENSP00000484033.1:p.Ala532Thr