Canonical Allele Identifier: CA10436655
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 1259529
ClinVar RCV Id: RCV001673905
dbSNP Id: rs5031002

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67722783G>A , CM000685.2:g.67722783G>A GRCh38
NC_000023.10:g.66942625G>A , CM000685.1:g.66942625G>A GRCh37
NC_000023.9:g.66859350G>A NCBI36
NG_009014.2:g.183752G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374690.9:c.2450-44G>A MANE Select ENSP00000363822.3:n.2450-44G>A
ENST00000396043.3:n.1077-44G>A ENSP00000379358.3:n.1077-44G>A
ENST00000396044.8:c.2174-903G>A ENSP00000379359.3:n.2174-903G>A
ENST00000612452.5:c.2450-44G>A ENSP00000484033.2:n.2450-44G>A
ENST00000374690.7:c.2450-44G>A ENSP00000363822.3:n.2450-44G>A
ENST00000396043.2:c.854-44G>A ENSP00000379358.2:n.854-44G>A
ENST00000396044.7:c.2174-903G>A ENSP00000379359.3:n.2174-903G>A
ENST00000612452.4:c.1901-44G>A ENSP00000484033.1:n.1901-44G>A
NM_000044.3:c.2450-44G>A NP_000035.2:n.2450-44G>A
NM_001011645.2:c.854-44G>A NP_001011645.1:n.854-44G>A
NM_000044.4:c.2450-44G>A NP_000035.2:n.2450-44G>A
NM_001011645.3:c.854-44G>A NP_001011645.1:n.854-44G>A
NM_000044.6:c.2450-44G>A MANE Select NP_000035.2:n.2450-44G>A