Canonical Allele Identifier: CA413423342

Gene: AR

Linked Data

• dbSNP Id: rs137852599
• MyVariant Identifiers: chrX:g.66931427A>G (hg19) ; chrX:g.67711585A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711585A>G , CM000685.2:g.67711585A>G	GRCh38
NC_000023.10:g.66931427A>G , CM000685.1:g.66931427A>G	GRCh37
NC_000023.9:g.66848152A>G	NCBI36
NG_009014.2:g.172554A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*417A>G	ENSP00000379358.4:n.*417A>G
ENST00000374690.9:c.2069A>G MANE Select	ENSP00000363822.3:p.His690Arg
ENST00000396043.3:c.696A>G	ENSP00000379358.3:n.696A>G
ENST00000396044.8:c.2069A>G	ENSP00000379359.3:p.His690Arg
ENST00000612452.5:c.2069A>G	ENSP00000484033.2:p.His690Arg
ENST00000374690.7:c.2069A>G	ENSP00000363822.3:p.His690Arg
ENST00000396043.2:c.473A>G	ENSP00000379358.2:p.His158Arg
ENST00000396044.7:c.2069A>G	ENSP00000379359.3:p.His690Arg
ENST00000612452.4:c.1499A>G	ENSP00000484033.1:p.His500Arg
NM_000044.3:c.2069A>G	NP_000035.2:p.His690Arg
NM_001011645.2:c.473A>G	NP_001011645.1:p.His158Arg
NM_000044.4:c.2069A>G	NP_000035.2:p.His690Arg
NM_001011645.3:c.473A>G	NP_001011645.1:p.His158Arg
NM_000044.6:c.2069A>G MANE Select	NP_000035.2:p.His690Arg