Canonical Allele Identifier: CA1204404975

Gene: RXRG

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165406806T>A , CM000663.2:g.165406806T>A	GRCh38
NC_000001.10:g.165376043T>A , CM000663.1:g.165376043T>A	GRCh37
NC_000001.9:g.163642667T>A	NCBI36
NG_029517.1:g.43550A>T
NG_029517.2:g.43550A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.1244+6A>T MANE Select	ENSP00000352900.5:n.1244+6A>T
ENST00000359842.9:c.1244+6A>T	ENSP00000352900.5:n.1244+6A>T
ENST00000619224.1:c.875+6A>T	ENSP00000482458.1:n.875+6A>T
NM_001256570.1:c.875+6A>T	NP_001243499.1:n.875+6A>T
NM_001256571.1:c.875+6A>T	NP_001243500.1:n.875+6A>T
NM_006917.4:c.1244+6A>T	NP_008848.1:n.1244+6A>T
NM_006917.5:c.1244+6A>T MANE Select	NP_008848.1:n.1244+6A>T
NM_001256571.2:c.875+6A>T	NP_001243500.1:n.875+6A>T
NM_001256570.2:c.875+6A>T	NP_001243499.1:n.875+6A>T