Canonical Allele Identifier: CA467648675

Gene: RXRA

Linked Data

• dbSNP Id: rs1831088922
• MyVariant Identifiers: chr9:g.137300069G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408223G>A , CM000671.2:g.134408223G>A	GRCh38
NC_000009.11:g.137300069G>A , CM000671.1:g.137300069G>A	GRCh37
NC_000009.10:g.136439890G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.354G>A MANE Select	ENSP00000419692.1:p.Lys118=
ENST00000672570.1:c.273G>A	ENSP00000500402.1:p.Lys91=
ENST00000356384.4:n.764G>A
ENST00000481739.1:c.354G>A	ENSP00000419692.1:p.Lys118=
NM_001291920.1:c.273G>A	NP_001278849.1:p.Lys91=
NM_001291921.1:c.63G>A	NP_001278850.1:p.Lys21=
NM_002957.5:c.354G>A	NP_002948.1:p.Lys118=
NM_002957.6:c.354G>A MANE Select	NP_002948.1:p.Lys118=
NM_001291921.2:c.63G>A	NP_001278850.1:p.Lys21=
NM_001291920.2:c.273G>A	NP_001278849.1:p.Lys91=