Canonical Allele Identifier: CA343472899

Gene: RXRG

Linked Data

• dbSNP Id: rs1452854810
• gnomAD v4: 1-165419922-G-T
• MyVariant Identifiers: chr1:g.165389159G>T (hg19) ; chr1:g.165419922G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419922G>T , CM000663.2:g.165419922G>T	GRCh38
NC_000001.10:g.165389159G>T , CM000663.1:g.165389159G>T	GRCh37
NC_000001.9:g.163655783G>T	NCBI36
NG_029517.1:g.30434C>A
NG_029517.2:g.30434C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.390C>A MANE Select	ENSP00000352900.5:p.Ser130Arg
ENST00000359842.9:c.390C>A	ENSP00000352900.5:p.Ser130Arg
ENST00000470566.1:n.315C>A
ENST00000619224.1:c.21C>A	ENSP00000482458.1:p.Ser7Arg
NM_001256570.1:c.21C>A	NP_001243499.1:p.Ser7Arg
NM_001256571.1:c.21C>A	NP_001243500.1:p.Ser7Arg
NM_006917.4:c.390C>A	NP_008848.1:p.Ser130Arg
NM_006917.5:c.390C>A MANE Select	NP_008848.1:p.Ser130Arg
NM_001256571.2:c.21C>A	NP_001243500.1:p.Ser7Arg
NM_001256570.2:c.21C>A	NP_001243499.1:p.Ser7Arg