Canonical Allele Identifier: CA2579630599
Gene: AR HGNC NCBI

Linked Data

dbSNP Id: rs2147530239
gnomAD v4: X-67717395-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67717395G>A , CM000685.2:g.67717395G>A GRCh38
NC_000023.10:g.66937237G>A , CM000685.1:g.66937237G>A GRCh37
NC_000023.9:g.66853962G>A NCBI36
NG_009014.2:g.178364G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*522-83G>A ENSP00000379358.4:n.*522-83G>A
ENST00000374690.9:c.2174-83G>A MANE Select ENSP00000363822.3:n.2174-83G>A
ENST00000396043.3:c.801-83G>A ENSP00000379358.3:n.801-83G>A
ENST00000396044.8:c.2173+5706G>A ENSP00000379359.3:n.2173+5706G>A
ENST00000612452.5:c.2174-83G>A ENSP00000484033.2:n.2174-83G>A
ENST00000374690.7:c.2174-83G>A ENSP00000363822.3:n.2174-83G>A
ENST00000396043.2:c.578-83G>A ENSP00000379358.2:n.578-83G>A
ENST00000396044.7:c.2173+5706G>A ENSP00000379359.3:n.2173+5706G>A
ENST00000612452.4:c.1604-83G>A ENSP00000484033.1:n.1604-83G>A
NM_000044.3:c.2174-83G>A NP_000035.2:n.2174-83G>A
NM_001011645.2:c.578-83G>A NP_001011645.1:n.578-83G>A
NM_000044.4:c.2174-83G>A NP_000035.2:n.2174-83G>A
NM_001011645.3:c.578-83G>A NP_001011645.1:n.578-83G>A
NM_000044.6:c.2174-83G>A MANE Select NP_000035.2:n.2174-83G>A