Canonical Allele Identifier: CA16621467

Gene: AR

Linked Data

• ClinVar Variation Id: 419726
• ClinVar RCV Id: RCV000482716
• dbSNP Id: rs1064794069
• MyVariant Identifiers: chrX:g.66942668G>A (hg19) ; chrX:g.67722826G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722826G>A , CM000685.2:g.67722826G>A	GRCh38
NC_000023.10:g.66942668G>A , CM000685.1:g.66942668G>A	GRCh37
NC_000023.9:g.66859393G>A	NCBI36
NG_009014.2:g.183795G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*798-1G>A	ENSP00000379358.4:n.*798-1G>A
ENST00000374690.9:c.2450-1G>A MANE Select	ENSP00000363822.3:n.2450-1G>A
ENST00000396043.3:c.1077-1G>A	ENSP00000379358.3:n.1077-1G>A
ENST00000396044.8:c.2174-860G>A	ENSP00000379359.3:n.2174-860G>A
ENST00000612452.5:c.2450-1G>A	ENSP00000484033.2:n.2450-1G>A
ENST00000374690.7:c.2450-1G>A	ENSP00000363822.3:n.2450-1G>A
ENST00000396043.2:c.854-1G>A	ENSP00000379358.2:n.854-1G>A
ENST00000396044.7:c.2174-860G>A	ENSP00000379359.3:n.2174-860G>A
ENST00000612452.4:c.1901-1G>A	ENSP00000484033.1:n.1901-1G>A
NM_000044.3:c.2450-1G>A	NP_000035.2:n.2450-1G>A
NM_001011645.2:c.854-1G>A	NP_001011645.1:n.854-1G>A
NM_000044.4:c.2450-1G>A	NP_000035.2:n.2450-1G>A
NM_001011645.3:c.854-1G>A	NP_001011645.1:n.854-1G>A
NM_000044.6:c.2450-1G>A MANE Select	NP_000035.2:n.2450-1G>A