Canonical Allele Identifier: CA343472817

Gene: RXRG

Linked Data

• gnomAD v4: 1-165419884-C-A
• MyVariant Identifiers: chr1:g.165389121C>A (hg19) ; chr1:g.165419884C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419884C>A , CM000663.2:g.165419884C>A	GRCh38
NC_000001.10:g.165389121C>A , CM000663.1:g.165389121C>A	GRCh37
NC_000001.9:g.163655745C>A	NCBI36
NG_029517.1:g.30472G>T
NG_029517.2:g.30472G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.428G>T MANE Select	ENSP00000352900.5:p.Gly143Val
ENST00000359842.9:c.428G>T	ENSP00000352900.5:p.Gly143Val
ENST00000470566.1:n.353G>T
ENST00000619224.1:c.59G>T	ENSP00000482458.1:p.Gly20Val
NM_001256570.1:c.59G>T	NP_001243499.1:p.Gly20Val
NM_001256571.1:c.59G>T	NP_001243500.1:p.Gly20Val
NM_006917.4:c.428G>T	NP_008848.1:p.Gly143Val
NM_006917.5:c.428G>T MANE Select	NP_008848.1:p.Gly143Val
NM_001256571.2:c.59G>T	NP_001243500.1:p.Gly20Val
NM_001256570.2:c.59G>T	NP_001243499.1:p.Gly20Val