Canonical Allele Identifier: CA120721

Gene: AR

Linked Data

• ClinVar Variation Id: 9823
• ClinVar RCV Id: RCV000010497 ; RCV000532628 ; RCV000582251
• dbSNP Id: rs9332971
• MyVariant Identifiers: chrX:g.66942786G>A (hg19) ; chrX:g.67722944G>A (hg38)
• PubMed: PMID:8097257

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722944G>A , CM000685.2:g.67722944G>A	GRCh38
NC_000023.10:g.66942786G>A , CM000685.1:g.66942786G>A	GRCh37
NC_000023.9:g.66859511G>A	NCBI36
NG_009014.2:g.183913G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*915G>A	ENSP00000379358.4:n.*915G>A
ENST00000374690.9:c.2567G>A MANE Select	ENSP00000363822.3:p.Arg856His
ENST00000396043.3:c.1194G>A	ENSP00000379358.3:n.1194G>A
ENST00000396044.8:c.2174-742G>A	ENSP00000379359.3:n.2174-742G>A
ENST00000612452.5:c.2567G>A	ENSP00000484033.2:p.Arg856His
ENST00000374690.7:c.2567G>A	ENSP00000363822.3:p.Arg856His
ENST00000396043.2:c.971G>A	ENSP00000379358.2:p.Arg324His
ENST00000396044.7:c.2174-742G>A	ENSP00000379359.3:n.2174-742G>A
ENST00000612452.4:c.2018G>A	ENSP00000484033.1:p.Arg673His
NM_000044.3:c.2567G>A	NP_000035.2:p.Arg856His
NM_001011645.2:c.971G>A	NP_001011645.1:p.Arg324His
NM_000044.4:c.2567G>A	NP_000035.2:p.Arg856His
NM_001011645.3:c.971G>A	NP_001011645.1:p.Arg324His
NM_000044.6:c.2567G>A MANE Select	NP_000035.2:p.Arg856His