Canonical Allele Identifier: CA516970637

Gene: AR

Linked Data

• ClinVar Variation Id: 2922967
• ClinVar RCV Id: RCV003788133
• dbSNP Id: rs2076137271
• gnomAD v3: X-67721851-C-G
• gnomAD v4: X-67721851-C-G
• MyVariant Identifiers: chrX:g.66941693C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721851C>G , CM000685.2:g.67721851C>G	GRCh38
NC_000023.10:g.66941693C>G , CM000685.1:g.66941693C>G	GRCh37
NC_000023.9:g.66858418C>G	NCBI36
NG_009014.2:g.182820C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*685C>G	ENSP00000379358.4:n.*685C>G
ENST00000374690.9:c.2337C>G MANE Select	ENSP00000363822.3:p.Ser779=
ENST00000396043.3:c.964C>G	ENSP00000379358.3:n.964C>G
ENST00000396044.8:c.2174-1835C>G	ENSP00000379359.3:n.2174-1835C>G
ENST00000612452.5:c.2337C>G	ENSP00000484033.2:p.Ser779=
ENST00000374690.7:c.2337C>G	ENSP00000363822.3:p.Ser779=
ENST00000396043.2:c.741C>G	ENSP00000379358.2:p.Ser247=
ENST00000396044.7:c.2174-1835C>G	ENSP00000379359.3:n.2174-1835C>G
ENST00000612452.4:c.1767C>G	ENSP00000484033.1:p.Ser589=
NM_000044.3:c.2337C>G	NP_000035.2:p.Ser779=
NM_001011645.2:c.741C>G	NP_001011645.1:p.Ser247=
NM_000044.4:c.2337C>G	NP_000035.2:p.Ser779=
NM_001011645.3:c.741C>G	NP_001011645.1:p.Ser247=
NM_000044.6:c.2337C>G MANE Select	NP_000035.2:p.Ser779=