Canonical Allele Identifier: CA120706
Gene: AR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9814
ClinVar RCV Id: RCV000010488
dbSNP Id: rs137852570

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721876A>G , CM000685.2:g.67721876A>G GRCh38
NC_000023.9:g.66858443A>G NCBI36
NC_000023.10:g.66941718A>G , CM000685.1:g.66941718A>G GRCh37
NG_009014.2:g.182845A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374690.7:c.2362A>G ENSP00000363822.3:p.Met788Val
ENST00000396043.2:c.766A>G ENSP00000379358.2:p.Met256Val
ENST00000396044.7:c.2174-1810A>G ENSP00000379359.3:p.=
ENST00000612452.4:c.1792A>G ENSP00000484033.1:p.Met598Val
NM_000044.3:c.2362A>G VV NP_000035.2:p.Met788Val
NM_001011645.2:c.766A>G VV NP_001011645.1:p.Met256Val