Canonical Allele Identifier: CA642377044

Gene: AR

Linked Data

• dbSNP Id: rs1241573634
• gnomAD v2: X-66937149-A-C
• gnomAD v3: X-67717307-A-C
• gnomAD v4: X-67717307-A-C
• MyVariant Identifiers: chrX:g.66937149A>C (hg19) ; chrX:g.67717307A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717307A>C , CM000685.2:g.67717307A>C	GRCh38
NC_000023.10:g.66937149A>C , CM000685.1:g.66937149A>C	GRCh37
NC_000023.9:g.66853874A>C	NCBI36
NG_009014.2:g.178276A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*522-171A>C	ENSP00000379358.4:n.*522-171A>C
ENST00000374690.9:c.2174-171A>C MANE Select	ENSP00000363822.3:n.2174-171A>C
ENST00000396043.3:c.801-171A>C	ENSP00000379358.3:n.801-171A>C
ENST00000396044.8:c.2173+5618A>C	ENSP00000379359.3:n.2173+5618A>C
ENST00000612452.5:c.2174-171A>C	ENSP00000484033.2:n.2174-171A>C
ENST00000374690.7:c.2174-171A>C	ENSP00000363822.3:n.2174-171A>C
ENST00000396043.2:c.578-171A>C	ENSP00000379358.2:n.578-171A>C
ENST00000396044.7:c.2173+5618A>C	ENSP00000379359.3:n.2173+5618A>C
ENST00000612452.4:c.1604-171A>C	ENSP00000484033.1:n.1604-171A>C
NM_000044.3:c.2174-171A>C	NP_000035.2:n.2174-171A>C
NM_001011645.2:c.578-171A>C	NP_001011645.1:n.578-171A>C
NM_000044.4:c.2174-171A>C	NP_000035.2:n.2174-171A>C
NM_001011645.3:c.578-171A>C	NP_001011645.1:n.578-171A>C
NM_000044.6:c.2174-171A>C MANE Select	NP_000035.2:n.2174-171A>C