Canonical Allele Identifier: CA10436630
Gene: AR HGNC NCBI

Linked Data

dbSNP Id: rs137852565
gnomAD v2: X-66941747-G-C
gnomAD v4: X-67721905-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721905G>C , CM000685.2:g.67721905G>C GRCh38
NC_000023.10:g.66941747G>C , CM000685.1:g.66941747G>C GRCh37
NC_000023.9:g.66858472G>C NCBI36
NG_009014.2:g.182874G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*739G>C ENSP00000379358.4:n.*739G>C
ENST00000374690.9:c.2391G>C MANE Select ENSP00000363822.3:p.Trp797Cys
ENST00000396043.3:c.1018G>C ENSP00000379358.3:n.1018G>C
ENST00000396044.8:c.2174-1781G>C ENSP00000379359.3:n.2174-1781G>C
ENST00000612452.5:c.2391G>C ENSP00000484033.2:p.Trp797Cys
ENST00000374690.7:c.2391G>C ENSP00000363822.3:p.Trp797Cys
ENST00000396043.2:c.795G>C ENSP00000379358.2:p.Trp265Cys
ENST00000396044.7:c.2174-1781G>C ENSP00000379359.3:n.2174-1781G>C
ENST00000612452.4:c.1821G>C ENSP00000484033.1:p.Trp607Cys
NM_000044.3:c.2391G>C NP_000035.2:p.Trp797Cys
NM_001011645.2:c.795G>C NP_001011645.1:p.Trp265Cys
NM_000044.4:c.2391G>C NP_000035.2:p.Trp797Cys
NM_001011645.3:c.795G>C NP_001011645.1:p.Trp265Cys
NM_000044.6:c.2391G>C MANE Select NP_000035.2:p.Trp797Cys