Canonical Allele Identifier: CA421567624

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389168T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419931T>A , CM000663.2:g.165419931T>A	GRCh38
NC_000001.10:g.165389168T>A , CM000663.1:g.165389168T>A	GRCh37
NC_000001.9:g.163655792T>A	NCBI36
NG_029517.1:g.30425A>T
NG_029517.2:g.30425A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.381A>T MANE Select	ENSP00000352900.5:p.Pro127=
ENST00000359842.9:c.381A>T	ENSP00000352900.5:p.Pro127=
ENST00000470566.1:n.306A>T
ENST00000619224.1:c.12A>T	ENSP00000482458.1:p.Pro4=
NM_001256570.1:c.12A>T	NP_001243499.1:p.Pro4=
NM_001256571.1:c.12A>T	NP_001243500.1:p.Pro4=
NM_006917.4:c.381A>T	NP_008848.1:p.Pro127=
NM_006917.5:c.381A>T MANE Select	NP_008848.1:p.Pro127=
NM_001256571.2:c.12A>T	NP_001243500.1:p.Pro4=
NM_001256570.2:c.12A>T	NP_001243499.1:p.Pro4=