Canonical Allele Identifier: CA32223399

Gene: RXRG

Linked Data

• dbSNP Id: rs943187807
• MyVariant Identifiers: chr1:g.165408959C>A (hg19) ; chr1:g.165439722C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439722C>A , CM000663.2:g.165439722C>A	GRCh38
NC_000001.10:g.165408959C>A , CM000663.1:g.165408959C>A	GRCh37
NC_000001.9:g.163675583C>A	NCBI36
NG_029517.1:g.10634G>T
NG_029517.2:g.10634G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+5123G>T MANE Select	ENSP00000352900.5:n.49+5123G>T
ENST00000359842.9:c.49+5123G>T	ENSP00000352900.5:n.49+5123G>T
ENST00000465764.1:n.329-2521G>T
ENST00000619224.1:c.-379+5123G>T	ENSP00000482458.1:n.-379+5123G>T
NM_001256570.1:c.-379+5123G>T	NP_001243499.1:n.-379+5123G>T
NM_006917.4:c.49+5123G>T	NP_008848.1:n.49+5123G>T
NR_033824.1:n.512-2521G>T
NM_006917.5:c.49+5123G>T MANE Select	NP_008848.1:n.49+5123G>T
NR_033824.2:n.283-2521G>T
NM_001256570.2:c.-379+5123G>T	NP_001243499.1:n.-379+5123G>T