Canonical Allele Identifier: CA1008685381

Gene: RXRG

Linked Data

• dbSNP Id: rs1658929480
• gnomAD v3: 1-165439954-G-A
• gnomAD v4: 1-165439954-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439954G>A , CM000663.2:g.165439954G>A	GRCh38
NC_000001.10:g.165409191G>A , CM000663.1:g.165409191G>A	GRCh37
NC_000001.9:g.163675815G>A	NCBI36
NG_029517.1:g.10402C>T
NG_029517.2:g.10402C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+4891C>T MANE Select	ENSP00000352900.5:n.49+4891C>T
ENST00000359842.9:c.49+4891C>T	ENSP00000352900.5:n.49+4891C>T
ENST00000465764.1:n.329-2753C>T
ENST00000619224.1:c.-379+4891C>T	ENSP00000482458.1:n.-379+4891C>T
NM_001256570.1:c.-379+4891C>T	NP_001243499.1:n.-379+4891C>T
NM_006917.4:c.49+4891C>T	NP_008848.1:n.49+4891C>T
NR_033824.1:n.512-2753C>T
NM_006917.5:c.49+4891C>T MANE Select	NP_008848.1:n.49+4891C>T
NR_033824.2:n.283-2753C>T
NM_001256570.2:c.-379+4891C>T	NP_001243499.1:n.-379+4891C>T