Canonical Allele Identifier: CA10436600
Gene: AR HGNC NCBI

Linked Data

dbSNP Id: rs749571801
gnomAD v2: X-66937329-A-G
gnomAD v3: X-67717487-A-G
gnomAD v4: X-67717487-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67717487A>G , CM000685.2:g.67717487A>G GRCh38
NC_000023.10:g.66937329A>G , CM000685.1:g.66937329A>G GRCh37
NC_000023.9:g.66854054A>G NCBI36
NG_009014.2:g.178456A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.*531A>G ENSP00000379358.4:n.*531A>G
ENST00000374690.9:c.2183A>G MANE Select ENSP00000363822.3:p.Asn728Ser
ENST00000396043.3:c.810A>G ENSP00000379358.3:n.810A>G
ENST00000396044.8:c.2173+5798A>G ENSP00000379359.3:n.2173+5798A>G
ENST00000612452.5:c.2183A>G ENSP00000484033.2:p.Asn728Ser
ENST00000374690.7:c.2183A>G ENSP00000363822.3:p.Asn728Ser
ENST00000396043.2:c.587A>G ENSP00000379358.2:p.Asn196Ser
ENST00000396044.7:c.2173+5798A>G ENSP00000379359.3:n.2173+5798A>G
ENST00000612452.4:c.1613A>G ENSP00000484033.1:p.Asn538Ser
NM_000044.3:c.2183A>G NP_000035.2:p.Asn728Ser
NM_001011645.2:c.587A>G NP_001011645.1:p.Asn196Ser
NM_000044.4:c.2183A>G NP_000035.2:p.Asn728Ser
NM_001011645.3:c.587A>G NP_001011645.1:p.Asn196Ser
NM_000044.6:c.2183A>G MANE Select NP_000035.2:p.Asn728Ser