Canonical Allele Identifier: CA343472876

Gene: RXRG

Linked Data

• ClinVar Variation Id: 3157310
• ClinVar RCV Id: RCV004447153
• MyVariant Identifiers: chr1:g.165389146C>A (hg19) ; chr1:g.165419909C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419909C>A , CM000663.2:g.165419909C>A	GRCh38
NC_000001.10:g.165389146C>A , CM000663.1:g.165389146C>A	GRCh37
NC_000001.9:g.163655770C>A	NCBI36
NG_029517.1:g.30447G>T
NG_029517.2:g.30447G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.403G>T MANE Select	ENSP00000352900.5:p.Val135Phe
ENST00000359842.9:c.403G>T	ENSP00000352900.5:p.Val135Phe
ENST00000470566.1:n.328G>T
ENST00000619224.1:c.34G>T	ENSP00000482458.1:p.Val12Phe
NM_001256570.1:c.34G>T	NP_001243499.1:p.Val12Phe
NM_001256571.1:c.34G>T	NP_001243500.1:p.Val12Phe
NM_006917.4:c.403G>T	NP_008848.1:p.Val135Phe
NM_006917.5:c.403G>T MANE Select	NP_008848.1:p.Val135Phe
NM_001256571.2:c.34G>T	NP_001243500.1:p.Val12Phe
NM_001256570.2:c.34G>T	NP_001243499.1:p.Val12Phe