Canonical Allele Identifier: CA120777

Gene: AR

Linked Data

• ClinVar Variation Id: 9847
• ClinVar RCV Id: RCV000010521 ; RCV003133116
• dbSNP Id: rs137852592
• MyVariant Identifiers: chrX:g.66941779T>C (hg19) ; chrX:g.67721937T>C (hg38)
• PubMed: PMID:10543676

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721937T>C , CM000685.2:g.67721937T>C	GRCh38
NC_000023.10:g.66941779T>C , CM000685.1:g.66941779T>C	GRCh37
NC_000023.9:g.66858504T>C	NCBI36
NG_009014.2:g.182906T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*771T>C	ENSP00000379358.4:n.*771T>C
ENST00000374690.9:c.2423T>C MANE Select	ENSP00000363822.3:p.Met808Thr
ENST00000396043.3:c.1050T>C	ENSP00000379358.3:n.1050T>C
ENST00000396044.8:c.2174-1749T>C	ENSP00000379359.3:n.2174-1749T>C
ENST00000612452.5:c.2423T>C	ENSP00000484033.2:p.Met808Thr
ENST00000374690.7:c.2423T>C	ENSP00000363822.3:p.Met808Thr
ENST00000396043.2:c.827T>C	ENSP00000379358.2:p.Met276Thr
ENST00000396044.7:c.2174-1749T>C	ENSP00000379359.3:n.2174-1749T>C
ENST00000612452.4:c.1853T>C	ENSP00000484033.1:p.Met618Thr
NM_000044.3:c.2423T>C	NP_000035.2:p.Met808Thr
NM_001011645.2:c.827T>C	NP_001011645.1:p.Met276Thr
NM_000044.4:c.2423T>C	NP_000035.2:p.Met808Thr
NM_001011645.3:c.827T>C	NP_001011645.1:p.Met276Thr
NM_000044.6:c.2423T>C MANE Select	NP_000035.2:p.Met808Thr