Canonical Allele Identifier: CA1204419592

Gene: RXRG

Linked Data

• dbSNP Id: rs1658920307

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439640T>C , CM000663.2:g.165439640T>C	GRCh38
NC_000001.10:g.165408877T>C , CM000663.1:g.165408877T>C	GRCh37
NC_000001.9:g.163675501T>C	NCBI36
NG_029517.1:g.10716A>G
NG_029517.2:g.10716A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+5205A>G MANE Select	ENSP00000352900.5:n.49+5205A>G
ENST00000359842.9:c.49+5205A>G	ENSP00000352900.5:n.49+5205A>G
ENST00000465764.1:n.329-2439A>G
ENST00000619224.1:c.-379+5205A>G	ENSP00000482458.1:n.-379+5205A>G
NM_001256570.1:c.-379+5205A>G	NP_001243499.1:n.-379+5205A>G
NM_006917.4:c.49+5205A>G	NP_008848.1:n.49+5205A>G
NR_033824.1:n.512-2439A>G
NM_006917.5:c.49+5205A>G MANE Select	NP_008848.1:n.49+5205A>G
NR_033824.2:n.283-2439A>G
NM_001256570.2:c.-379+5205A>G	NP_001243499.1:n.-379+5205A>G