Canonical Allele Identifier: CA527077812

Gene: RXRG

Linked Data

• dbSNP Id: rs1349498999
• gnomAD v2: 1-165389004-C-G
• gnomAD v3: 1-165419767-C-G
• gnomAD v4: 1-165419767-C-G
• MyVariant Identifiers: chr1:g.165389004C>G (hg19) ; chr1:g.165419767C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419767C>G , CM000663.2:g.165419767C>G	GRCh38
NC_000001.10:g.165389004C>G , CM000663.1:g.165389004C>G	GRCh37
NC_000001.9:g.163655628C>G	NCBI36
NG_029517.1:g.30589G>C
NG_029517.2:g.30589G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+103G>C MANE Select	ENSP00000352900.5:n.442+103G>C
ENST00000359842.9:c.442+103G>C	ENSP00000352900.5:n.442+103G>C
ENST00000470566.1:n.367+103G>C
ENST00000619224.1:c.73+103G>C	ENSP00000482458.1:n.73+103G>C
NM_001256570.1:c.73+103G>C	NP_001243499.1:n.73+103G>C
NM_001256571.1:c.73+103G>C	NP_001243500.1:n.73+103G>C
NM_006917.4:c.442+103G>C	NP_008848.1:n.442+103G>C
NM_006917.5:c.442+103G>C MANE Select	NP_008848.1:n.442+103G>C
NM_001256571.2:c.73+103G>C	NP_001243500.1:n.73+103G>C
NM_001256570.2:c.73+103G>C	NP_001243499.1:n.73+103G>C