Canonical Allele Identifier: CA1204410220
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165420163A= , CM000663.2:g.165420163A= GRCh38
NC_000001.10:g.165389400A= , CM000663.1:g.165389400A= GRCh37
NC_000001.9:g.163656024A= NCBI36
NG_029517.1:g.30193T=
NG_029517.2:g.30193T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.298-149T= MANE Select ENSP00000352900.5:n.298-149T=
ENST00000359842.9:c.298-149T= ENSP00000352900.5:n.298-149T=
ENST00000470566.1:n.223-149T=
ENST00000619224.1:c.-72-149T= ENSP00000482458.1:n.-72-149T=
NM_001256570.1:c.-72-149T= NP_001243499.1:n.-72-149T=
NM_001256571.1:c.-72-149T= NP_001243500.1:n.-72-149T=
NM_006917.4:c.298-149T= NP_008848.1:n.298-149T=
NM_006917.5:c.298-149T= MANE Select NP_008848.1:n.298-149T=
NM_001256571.2:c.-72-149T= NP_001243500.1:n.-72-149T=
NM_001256570.2:c.-72-149T= NP_001243499.1:n.-72-149T=