Canonical Allele Identifier: CA413424239
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 2000750
ClinVar RCV Id: RCV002802182
dbSNP Id: rs2147530549

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67717476A>G , CM000685.2:g.67717476A>G GRCh38
NC_000023.10:g.66937318A>G , CM000685.1:g.66937318A>G GRCh37
NC_000023.9:g.66854043A>G NCBI36
NG_009014.2:g.178445A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.*522-2A>G ENSP00000379358.4:n.*522-2A>G
ENST00000374690.9:c.2174-2A>G MANE Select ENSP00000363822.3:n.2174-2A>G
ENST00000396043.3:c.801-2A>G ENSP00000379358.3:n.801-2A>G
ENST00000396044.8:c.2173+5787A>G ENSP00000379359.3:n.2173+5787A>G
ENST00000612452.5:c.2174-2A>G ENSP00000484033.2:n.2174-2A>G
ENST00000374690.7:c.2174-2A>G ENSP00000363822.3:n.2174-2A>G
ENST00000396043.2:c.578-2A>G ENSP00000379358.2:n.578-2A>G
ENST00000396044.7:c.2173+5787A>G ENSP00000379359.3:n.2173+5787A>G
ENST00000612452.4:c.1604-2A>G ENSP00000484033.1:n.1604-2A>G
NM_000044.3:c.2174-2A>G NP_000035.2:n.2174-2A>G
NM_001011645.2:c.578-2A>G NP_001011645.1:n.578-2A>G
NM_000044.4:c.2174-2A>G NP_000035.2:n.2174-2A>G
NM_001011645.3:c.578-2A>G NP_001011645.1:n.578-2A>G
NM_000044.6:c.2174-2A>G MANE Select NP_000035.2:n.2174-2A>G