Canonical Allele Identifier: CA1204410154
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419999T= , CM000663.2:g.165419999T= GRCh38
NC_000001.10:g.165389236T= , CM000663.1:g.165389236T= GRCh37
NC_000001.9:g.163655860T= NCBI36
NG_029517.1:g.30357A=
NG_029517.2:g.30357A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.313A= MANE Select ENSP00000352900.5:p.Ser105=
ENST00000359842.9:c.313A= ENSP00000352900.5:p.Ser105=
ENST00000470566.1:n.238A=
ENST00000619224.1:c.-57A= ENSP00000482458.1:n.-57A=
NM_001256570.1:c.-57A= NP_001243499.1:n.-57A=
NM_001256571.1:c.-57A= NP_001243500.1:n.-57A=
NM_006917.4:c.313A= NP_008848.1:p.Ser105=
NM_006917.5:c.313A= MANE Select NP_008848.1:p.Ser105=
NM_001256571.2:c.-57A= NP_001243500.1:n.-57A=
NM_001256570.2:c.-57A= NP_001243499.1:n.-57A=