Canonical Allele Identifier: CA32223411
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs10800098

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439858G>A , CM000663.2:g.165439858G>A GRCh38
NC_000001.10:g.165409095G>A , CM000663.1:g.165409095G>A GRCh37
NC_000001.9:g.163675719G>A NCBI36
NG_029517.1:g.10498C>T
NG_029517.2:g.10498C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+4987C>T MANE Select ENSP00000352900.5:n.49+4987C>T
ENST00000359842.9:c.49+4987C>T ENSP00000352900.5:n.49+4987C>T
ENST00000465764.1:n.329-2657C>T
ENST00000619224.1:c.-379+4987C>T ENSP00000482458.1:n.-379+4987C>T
NM_001256570.1:c.-379+4987C>T NP_001243499.1:n.-379+4987C>T
NM_006917.4:c.49+4987C>T NP_008848.1:n.49+4987C>T
NR_033824.1:n.512-2657C>T
NM_006917.5:c.49+4987C>T MANE Select NP_008848.1:n.49+4987C>T
NR_033824.2:n.283-2657C>T
NM_001256570.2:c.-379+4987C>T NP_001243499.1:n.-379+4987C>T