Canonical Allele Identifier: CA1204410138
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419952C= , CM000663.2:g.165419952C= GRCh38
NC_000001.10:g.165389189C= , CM000663.1:g.165389189C= GRCh37
NC_000001.9:g.163655813C= NCBI36
NG_029517.1:g.30404G=
NG_029517.2:g.30404G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.360G= MANE Select ENSP00000352900.5:p.Gly120=
ENST00000359842.9:c.360G= ENSP00000352900.5:p.Gly120=
ENST00000470566.1:n.285G=
ENST00000619224.1:c.-10G= ENSP00000482458.1:n.-10G=
NM_001256570.1:c.-10G= NP_001243499.1:n.-10G=
NM_001256571.1:c.-10G= NP_001243500.1:n.-10G=
NM_006917.4:c.360G= NP_008848.1:p.Gly120=
NM_006917.5:c.360G= MANE Select NP_008848.1:p.Gly120=
NM_001256571.2:c.-10G= NP_001243500.1:n.-10G=
NM_001256570.2:c.-10G= NP_001243499.1:n.-10G=