Canonical Allele Identifier: CA2534766578

Gene: AR

Linked Data

• dbSNP Id: rs2147523820

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711326T>G , CM000685.2:g.67711326T>G	GRCh38
NC_000023.10:g.66931168T>G , CM000685.1:g.66931168T>G	GRCh37
NC_000023.9:g.66847893T>G	NCBI36
NG_009014.2:g.172295T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*234-76T>G	ENSP00000379358.4:n.*234-76T>G
ENST00000374690.9:c.1886-76T>G MANE Select	ENSP00000363822.3:n.1886-76T>G
ENST00000396043.3:c.513-76T>G	ENSP00000379358.3:n.513-76T>G
ENST00000396044.8:c.1886-76T>G	ENSP00000379359.3:n.1886-76T>G
ENST00000612452.5:c.1886-76T>G	ENSP00000484033.2:n.1886-76T>G
ENST00000374690.7:c.1886-76T>G	ENSP00000363822.3:n.1886-76T>G
ENST00000396043.2:c.290-76T>G	ENSP00000379358.2:n.290-76T>G
ENST00000396044.7:c.1886-76T>G	ENSP00000379359.3:n.1886-76T>G
ENST00000612452.4:c.1316-76T>G	ENSP00000484033.1:n.1316-76T>G
NM_000044.3:c.1886-76T>G	NP_000035.2:n.1886-76T>G
NM_001011645.2:c.290-76T>G	NP_001011645.1:n.290-76T>G
NM_000044.4:c.1886-76T>G	NP_000035.2:n.1886-76T>G
NM_001011645.3:c.290-76T>G	NP_001011645.1:n.290-76T>G
NM_000044.6:c.1886-76T>G MANE Select	NP_000035.2:n.1886-76T>G