Canonical Allele Identifier: CA517047660

Gene: AR

Linked Data

• dbSNP Id: rs2147314141
• gnomAD v4: X-67545239-C-G
• MyVariant Identifiers: chrX:g.66765081C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545239C>G , CM000685.2:g.67545239C>G	GRCh38
NC_000023.10:g.66765081C>G , CM000685.1:g.66765081C>G	GRCh37
NC_000023.9:g.66681806C>G	NCBI36
NG_009014.2:g.6208C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.93C>G	ENSP00000379358.4:p.Arg31=
ENST00000374690.9:c.93C>G MANE Select	ENSP00000363822.3:p.Arg31=
ENST00000396044.8:c.93C>G	ENSP00000379359.3:p.Arg31=
ENST00000612452.5:c.93C>G	ENSP00000484033.2:p.Arg31=
ENST00000374690.7:c.93C>G	ENSP00000363822.3:p.Arg31=
ENST00000396044.7:c.93C>G	ENSP00000379359.3:p.Arg31=
ENST00000504326.5:c.93C>G	ENSP00000421155.1:p.Arg31=
ENST00000513847.5:n.420C>G
ENST00000514029.5:c.93C>G	ENSP00000425199.1:p.Arg31=
ENST00000612010.4:c.93C>G	ENSP00000482407.1:p.Arg31=
ENST00000612452.4:c.-478C>G	ENSP00000484033.1:n.-478C>G
ENST00000613054.2:c.93C>G	ENSP00000479013.1:p.Arg31=
NM_000044.3:c.93C>G	NP_000035.2:p.Arg31=
NM_000044.4:c.93C>G	NP_000035.2:p.Arg31=
NM_001011645.3:c.-1691C>G	NP_001011645.1:n.-1691C>G
NM_001348061.1:c.93C>G	NP_001334990.1:p.Arg31=
NM_001348063.1:c.93C>G	NP_001334992.1:p.Arg31=
NM_001348064.1:c.93C>G	NP_001334993.1:p.Arg31=
NM_000044.6:c.93C>G MANE Select	NP_000035.2:p.Arg31=