Canonical Allele Identifier: CA2648887552

Gene: RXRG

Linked Data

• gnomAD v4: 1-165419792-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419792A>G , CM000663.2:g.165419792A>G	GRCh38
NC_000001.10:g.165389029A>G , CM000663.1:g.165389029A>G	GRCh37
NC_000001.9:g.163655653A>G	NCBI36
NG_029517.1:g.30564T>C
NG_029517.2:g.30564T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000359842.10:c.442+78T>C MANE Select	ENSP00000352900.5:n.442+78T>C
ENST00000359842.9:c.442+78T>C	ENSP00000352900.5:n.442+78T>C
ENST00000470566.1:n.367+78T>C
ENST00000619224.1:c.73+78T>C	ENSP00000482458.1:n.73+78T>C
NM_001256570.1:c.73+78T>C	NP_001243499.1:n.73+78T>C
NM_001256571.1:c.73+78T>C	NP_001243500.1:n.73+78T>C
NM_006917.4:c.442+78T>C	NP_008848.1:n.442+78T>C
NM_006917.5:c.442+78T>C MANE Select	NP_008848.1:n.442+78T>C
NM_001256571.2:c.73+78T>C	NP_001243500.1:n.73+78T>C
NM_001256570.2:c.73+78T>C	NP_001243499.1:n.73+78T>C