Canonical Allele Identifier: CA343472873

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389145A>C (hg19) ; chr1:g.165419908A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419908A>C , CM000663.2:g.165419908A>C	GRCh38
NC_000001.10:g.165389145A>C , CM000663.1:g.165389145A>C	GRCh37
NC_000001.9:g.163655769A>C	NCBI36
NG_029517.1:g.30448T>G
NG_029517.2:g.30448T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.404T>G MANE Select	ENSP00000352900.5:p.Val135Gly
ENST00000359842.9:c.404T>G	ENSP00000352900.5:p.Val135Gly
ENST00000470566.1:n.329T>G
ENST00000619224.1:c.35T>G	ENSP00000482458.1:p.Val12Gly
NM_001256570.1:c.35T>G	NP_001243499.1:p.Val12Gly
NM_001256571.1:c.35T>G	NP_001243500.1:p.Val12Gly
NM_006917.4:c.404T>G	NP_008848.1:p.Val135Gly
NM_006917.5:c.404T>G MANE Select	NP_008848.1:p.Val135Gly
NM_001256571.2:c.35T>G	NP_001243500.1:p.Val12Gly
NM_001256570.2:c.35T>G	NP_001243499.1:p.Val12Gly