Canonical Allele Identifier: CA120703
Gene: AR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9813
dbSNP Id: rs137852569

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67686030G>A , CM000685.2:g.67686030G>A GRCh38
NC_000023.10:g.66905872G>A , CM000685.1:g.66905872G>A GRCh37
NC_000023.9:g.66822597G>A NCBI36
NG_009014.2:g.146999G>A

Transcript Alleles

HGVS Amino-acid change
NM_000044.3:c.1789G>A VV NP_000035.2:p.Ala597Thr
NM_001011645.2:c.193G>A VV NP_001011645.1:p.Ala65Thr
NM_000044.4:c.1789G>A VV NP_000035.2:p.Ala597Thr
NM_001011645.3:c.193G>A VV NP_001011645.1:p.Ala65Thr
NM_001348061.1:c.1789G>A VV NP_001334990.1:p.Ala597Thr
NM_001348063.1:c.1789G>A VV NP_001334992.1:p.Ala597Thr
NM_001348064.1:c.1706G>A VV NP_001334993.1:p.Arg569His
ENST00000374690.7:c.1789G>A ENSP00000363822.3:p.Ala597Thr
ENST00000396043.2:c.193G>A ENSP00000379358.2:p.Ala65Thr
ENST00000396044.7:c.1789G>A ENSP00000379359.3:p.Ala597Thr
ENST00000504326.5:c.1789G>A ENSP00000421155.1:p.Ala597Thr
ENST00000513847.5:n.2116G>A
ENST00000514029.5:c.*270G>A ENSP00000425199.1:p.=
ENST00000612010.4:c.*141G>A ENSP00000482407.1:p.=
ENST00000612452.4:c.1219G>A ENSP00000484033.1:p.Ala407Thr
ENST00000613054.2:c.1706G>A ENSP00000479013.1:p.Arg569His