Canonical Allele Identifier: CA375452025

Gene: RXRA

Linked Data

• dbSNP Id: rs1158453429
• gnomAD v4: 9-134408167-C-A
• MyVariant Identifiers: chr9:g.137300013C>A (hg19) ; chr9:g.134408167C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408167C>A , CM000671.2:g.134408167C>A	GRCh38
NC_000009.11:g.137300013C>A , CM000671.1:g.137300013C>A	GRCh37
NC_000009.10:g.136439834C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.298C>A MANE Select	ENSP00000419692.1:p.Pro100Thr
ENST00000672570.1:c.217C>A	ENSP00000500402.1:p.Pro73Thr
ENST00000356384.4:n.708C>A
ENST00000481739.1:c.298C>A	ENSP00000419692.1:p.Pro100Thr
NM_001291920.1:c.217C>A	NP_001278849.1:p.Pro73Thr
NM_001291921.1:c.7C>A	NP_001278850.1:p.Pro3Thr
NM_002957.5:c.298C>A	NP_002948.1:p.Pro100Thr
NM_002957.6:c.298C>A MANE Select	NP_002948.1:p.Pro100Thr
NM_001291921.2:c.7C>A	NP_001278850.1:p.Pro3Thr
NM_001291920.2:c.217C>A	NP_001278849.1:p.Pro73Thr