Canonical Allele Identifier: CA890557446

Gene: RXRG

Linked Data

• dbSNP Id: rs1334886158
• gnomAD v3: 1-165439714-C-G
• gnomAD v4: 1-165439714-C-G
• MyVariant Identifiers: chr1:g.165408951C>G (hg19) ; chr1:g.165439714C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439714C>G , CM000663.2:g.165439714C>G	GRCh38
NC_000001.10:g.165408951C>G , CM000663.1:g.165408951C>G	GRCh37
NC_000001.9:g.163675575C>G	NCBI36
NG_029517.1:g.10642G>C
NG_029517.2:g.10642G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+5131G>C MANE Select	ENSP00000352900.5:n.49+5131G>C
ENST00000359842.9:c.49+5131G>C	ENSP00000352900.5:n.49+5131G>C
ENST00000465764.1:n.329-2513G>C
ENST00000619224.1:c.-379+5131G>C	ENSP00000482458.1:n.-379+5131G>C
NM_001256570.1:c.-379+5131G>C	NP_001243499.1:n.-379+5131G>C
NM_006917.4:c.49+5131G>C	NP_008848.1:n.49+5131G>C
NR_033824.1:n.512-2513G>C
NM_006917.5:c.49+5131G>C MANE Select	NP_008848.1:n.49+5131G>C
NR_033824.2:n.283-2513G>C
NM_001256570.2:c.-379+5131G>C	NP_001243499.1:n.-379+5131G>C