Canonical Allele Identifier: CA120726
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9825
ClinVar RCV Id: RCV000010499
dbSNP Id: rs137852575

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67545324C>T , CM000685.2:g.67545324C>T GRCh38
NC_000023.10:g.66765166C>T , CM000685.1:g.66765166C>T GRCh37
NC_000023.9:g.66681891C>T NCBI36
NG_009014.2:g.6293C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374690.9:c.178C>T MANE Select ENSP00000363822.3:p.Gln60Ter
ENST00000396044.8:c.178C>T ENSP00000379359.3:p.Gln60Ter
ENST00000612452.5:c.178C>T ENSP00000484033.2:p.Gln60Ter
ENST00000374690.7:c.178C>T ENSP00000363822.3:p.Gln60Ter
ENST00000396044.7:c.178C>T ENSP00000379359.3:p.Gln60Ter
ENST00000504326.5:c.178C>T ENSP00000421155.1:p.Gln60Ter
ENST00000513847.5:n.505C>T
ENST00000514029.5:c.178C>T ENSP00000425199.1:p.Gln60Ter
ENST00000612010.4:c.178C>T ENSP00000482407.1:p.Gln60Ter
ENST00000612452.4:c.-393C>T ENSP00000484033.1:p.=
ENST00000613054.2:c.178C>T ENSP00000479013.1:p.Gln60Ter
NM_000044.3:c.178C>T NP_000035.2:p.Gln60Ter
NM_000044.4:c.178C>T NP_000035.2:p.Gln60Ter
NM_001011645.3:c.-1606C>T NP_001011645.1:p.=
NM_001348061.1:c.178C>T NP_001334990.1:p.Gln60Ter
NM_001348063.1:c.178C>T NP_001334992.1:p.Gln60Ter
NM_001348064.1:c.178C>T NP_001334993.1:p.Gln60Ter
NM_000044.6:c.178C>T MANE Select NP_000035.2:p.Gln60Ter