Canonical Allele Identifier: CA120786

Gene: AR

Linked Data

• ClinVar Variation Id: 9857
• ClinVar RCV Id: RCV000010531 ; RCV000010532 ; RCV001851781
• dbSNP Id: rs137852600
• MyVariant Identifiers: chrX:g.66937377G>T (hg19) ; chrX:g.67717535G>T (hg38)
• PubMed: PMID:8096390 ; PMID:8325932

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717535G>T , CM000685.2:g.67717535G>T	GRCh38
NC_000023.10:g.66937377G>T , CM000685.1:g.66937377G>T	GRCh37
NC_000023.9:g.66854102G>T	NCBI36
NG_009014.2:g.178504G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*579G>T	ENSP00000379358.4:n.*579G>T
ENST00000374690.9:c.2231G>T MANE Select	ENSP00000363822.3:p.Gly744Val
ENST00000396043.3:c.858G>T	ENSP00000379358.3:n.858G>T
ENST00000396044.8:c.2173+5846G>T	ENSP00000379359.3:n.2173+5846G>T
ENST00000612452.5:c.2231G>T	ENSP00000484033.2:p.Gly744Val
ENST00000374690.7:c.2231G>T	ENSP00000363822.3:p.Gly744Val
ENST00000396043.2:c.635G>T	ENSP00000379358.2:p.Gly212Val
ENST00000396044.7:c.2173+5846G>T	ENSP00000379359.3:n.2173+5846G>T
ENST00000612452.4:c.1661G>T	ENSP00000484033.1:p.Gly554Val
NM_000044.3:c.2231G>T	NP_000035.2:p.Gly744Val
NM_001011645.2:c.635G>T	NP_001011645.1:p.Gly212Val
NM_000044.4:c.2231G>T	NP_000035.2:p.Gly744Val
NM_001011645.3:c.635G>T	NP_001011645.1:p.Gly212Val
NM_000044.6:c.2231G>T MANE Select	NP_000035.2:p.Gly744Val