Canonical Allele Identifier: CA254903
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9853
ClinVar RCV Id: RCV000010527
dbSNP Id: rs137852596

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67643371G>A , CM000685.2:g.67643371G>A GRCh38
NC_000023.10:g.66863213G>A , CM000685.1:g.66863213G>A GRCh37
NC_000023.9:g.66779938G>A NCBI36
NG_009014.2:g.104340G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374690.9:c.1732G>A MANE Select ENSP00000363822.3:p.Gly578Arg
ENST00000396043.3:n.359G>A ENSP00000379358.3:p.=
ENST00000396044.8:c.1732G>A ENSP00000379359.3:p.Gly578Arg
ENST00000612452.5:c.1732G>A ENSP00000484033.2:p.Gly578Arg
ENST00000374690.7:c.1732G>A ENSP00000363822.3:p.Gly578Arg
ENST00000396043.2:c.136G>A ENSP00000379358.2:p.Gly46Arg
ENST00000396044.7:c.1732G>A ENSP00000379359.3:p.Gly578Arg
ENST00000504326.5:c.1732G>A ENSP00000421155.1:p.Gly578Arg
ENST00000513847.5:n.2059G>A
ENST00000514029.5:c.1732G>A ENSP00000425199.1:p.Gly578Arg
ENST00000612010.4:c.1732G>A ENSP00000482407.1:p.Gly578Arg
ENST00000612452.4:c.1162G>A ENSP00000484033.1:p.Gly388Arg
ENST00000613054.2:c.1617-42570G>A ENSP00000479013.1:p.=
NM_000044.3:c.1732G>A NP_000035.2:p.Gly578Arg
NM_001011645.2:c.136G>A NP_001011645.1:p.Gly46Arg
NM_000044.4:c.1732G>A NP_000035.2:p.Gly578Arg
NM_001011645.3:c.136G>A NP_001011645.1:p.Gly46Arg
NM_001348061.1:c.1732G>A NP_001334990.1:p.Gly578Arg
NM_001348063.1:c.1732G>A NP_001334992.1:p.Gly578Arg
NM_001348064.1:c.1617-42570G>A NP_001334993.1:p.=
NM_000044.6:c.1732G>A MANE Select NP_000035.2:p.Gly578Arg