Canonical Allele Identifier: CA517048588

Gene: AR

Linked Data

• dbSNP Id: rs2147525185
• MyVariant Identifiers: chrX:g.66931491A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711649A>G , CM000685.2:g.67711649A>G	GRCh38
NC_000023.10:g.66931491A>G , CM000685.1:g.66931491A>G	GRCh37
NC_000023.9:g.66848216A>G	NCBI36
NG_009014.2:g.172618A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*481A>G	ENSP00000379358.4:n.*481A>G
ENST00000374690.9:c.2133A>G MANE Select	ENSP00000363822.3:p.Arg711=
ENST00000396043.3:c.760A>G	ENSP00000379358.3:n.760A>G
ENST00000396044.8:c.2133A>G	ENSP00000379359.3:p.Arg711=
ENST00000612452.5:c.2133A>G	ENSP00000484033.2:p.Arg711=
ENST00000374690.7:c.2133A>G	ENSP00000363822.3:p.Arg711=
ENST00000396043.2:c.537A>G	ENSP00000379358.2:p.Arg179=
ENST00000396044.7:c.2133A>G	ENSP00000379359.3:p.Arg711=
ENST00000612452.4:c.1563A>G	ENSP00000484033.1:p.Arg521=
NM_000044.3:c.2133A>G	NP_000035.2:p.Arg711=
NM_001011645.2:c.537A>G	NP_001011645.1:p.Arg179=
NM_000044.4:c.2133A>G	NP_000035.2:p.Arg711=
NM_001011645.3:c.537A>G	NP_001011645.1:p.Arg179=
NM_000044.6:c.2133A>G MANE Select	NP_000035.2:p.Arg711=