Canonical Allele Identifier: CA343472851
Gene: RXRG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419898G>C , CM000663.2:g.165419898G>C GRCh38
NC_000001.10:g.165389135G>C , CM000663.1:g.165389135G>C GRCh37
NC_000001.9:g.163655759G>C NCBI36
NG_029517.1:g.30458C>G
NG_029517.2:g.30458C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.414C>G MANE Select ENSP00000352900.5:p.Ile138Met
ENST00000359842.9:c.414C>G ENSP00000352900.5:p.Ile138Met
ENST00000470566.1:n.339C>G
ENST00000619224.1:c.45C>G ENSP00000482458.1:p.Ile15Met
NM_001256570.1:c.45C>G NP_001243499.1:p.Ile15Met
NM_001256571.1:c.45C>G NP_001243500.1:p.Ile15Met
NM_006917.4:c.414C>G NP_008848.1:p.Ile138Met
NM_006917.5:c.414C>G MANE Select NP_008848.1:p.Ile138Met
NM_001256571.2:c.45C>G NP_001243500.1:p.Ile15Met
NM_001256570.2:c.45C>G NP_001243499.1:p.Ile15Met