Canonical Allele Identifier: CA120734
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9830
ClinVar RCV Id: RCV000010504 RCV000010529 RCV000640474
dbSNP Id: rs137852577
gnomAD v4: X-67722898-C-T
MyVariant Identifiers: chrX:g.66942740C>T (hg19) chrX:g.67722898C>T (hg38)
PubMed: PMID:8040309 PMID:11788673
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67722898C>T , CM000685.2:g.67722898C>T GRCh38
NC_000023.10:g.66942740C>T , CM000685.1:g.66942740C>T GRCh37
NC_000023.9:g.66859465C>T NCBI36
NG_009014.2:g.183867C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*869C>T ENSP00000379358.4:n.*869C>T
ENST00000374690.9:c.2521C>T MANE Select ENSP00000363822.3:p.Arg841Cys
ENST00000396043.3:c.1148C>T ENSP00000379358.3:n.1148C>T
ENST00000396044.8:c.2174-788C>T ENSP00000379359.3:n.2174-788C>T
ENST00000612452.5:c.2521C>T ENSP00000484033.2:p.Arg841Cys
ENST00000374690.7:c.2521C>T ENSP00000363822.3:p.Arg841Cys
ENST00000396043.2:c.925C>T ENSP00000379358.2:p.Arg309Cys
ENST00000396044.7:c.2174-788C>T ENSP00000379359.3:n.2174-788C>T
ENST00000612452.4:c.1972C>T ENSP00000484033.1:p.Arg658Cys
NM_000044.3:c.2521C>T NP_000035.2:p.Arg841Cys
NM_001011645.2:c.925C>T NP_001011645.1:p.Arg309Cys
NM_000044.4:c.2521C>T NP_000035.2:p.Arg841Cys
NM_001011645.3:c.925C>T NP_001011645.1:p.Arg309Cys
NM_000044.6:c.2521C>T MANE Select NP_000035.2:p.Arg841Cys
Search 100 bp 5'
Search 100 bp 3'