Canonical Allele Identifier: CA1204410126
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419917C= , CM000663.2:g.165419917C= GRCh38
NC_000001.10:g.165389154C= , CM000663.1:g.165389154C= GRCh37
NC_000001.9:g.163655778C= NCBI36
NG_029517.1:g.30439G=
NG_029517.2:g.30439G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.395G= MANE Select ENSP00000352900.5:p.Gly132=
ENST00000359842.9:c.395G= ENSP00000352900.5:p.Gly132=
ENST00000470566.1:n.320G=
ENST00000619224.1:c.26G= ENSP00000482458.1:p.Gly9=
NM_001256570.1:c.26G= NP_001243499.1:p.Gly9=
NM_001256571.1:c.26G= NP_001243500.1:p.Gly9=
NM_006917.4:c.395G= NP_008848.1:p.Gly132=
NM_006917.5:c.395G= MANE Select NP_008848.1:p.Gly132=
NM_001256571.2:c.26G= NP_001243500.1:p.Gly9=
NM_001256570.2:c.26G= NP_001243499.1:p.Gly9=