Canonical Allele Identifier: CA10603629

Gene: AR

Linked Data

• ClinVar Variation Id: 280062
• ClinVar RCV Id: RCV000263998 ; RCV001175283
• dbSNP Id: rs886041352
• MyVariant Identifiers: chrX:g.66937460A>C (hg19) ; chrX:g.67717618A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717618A>C , CM000685.2:g.67717618A>C	GRCh38
NC_000023.10:g.66937460A>C , CM000685.1:g.66937460A>C	GRCh37
NC_000023.9:g.66854185A>C	NCBI36
NG_009014.2:g.178587A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*662A>C	ENSP00000379358.4:n.*662A>C
ENST00000374690.9:c.2314A>C MANE Select	ENSP00000363822.3:p.Asn772His
ENST00000396043.3:c.941A>C	ENSP00000379358.3:n.941A>C
ENST00000396044.8:c.2173+5929A>C	ENSP00000379359.3:n.2173+5929A>C
ENST00000612452.5:c.2314A>C	ENSP00000484033.2:p.Asn772His
ENST00000374690.7:c.2314A>C	ENSP00000363822.3:p.Asn772His
ENST00000396043.2:c.718A>C	ENSP00000379358.2:p.Asn240His
ENST00000396044.7:c.2173+5929A>C	ENSP00000379359.3:n.2173+5929A>C
ENST00000612452.4:c.1744A>C	ENSP00000484033.1:p.Asn582His
NM_000044.3:c.2314A>C	NP_000035.2:p.Asn772His
NM_001011645.2:c.718A>C	NP_001011645.1:p.Asn240His
NM_000044.4:c.2314A>C	NP_000035.2:p.Asn772His
NM_001011645.3:c.718A>C	NP_001011645.1:p.Asn240His
NM_000044.6:c.2314A>C MANE Select	NP_000035.2:p.Asn772His