Canonical Allele Identifier: CA5317708

Gene: RXRA

Linked Data

• dbSNP Id: rs765447006
• ExAC: 9:137300043 C / A
• gnomAD v2: 9-137300043-C-A
• gnomAD v4: 9-134408197-C-A
• MyVariant Identifiers: chr9:g.137300043C>A (hg19) ; chr9:g.134408197C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408197C>A , CM000671.2:g.134408197C>A	GRCh38
NC_000009.11:g.137300043C>A , CM000671.1:g.137300043C>A	GRCh37
NC_000009.10:g.136439864C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.328C>A MANE Select	ENSP00000419692.1:p.Pro110Thr
ENST00000672570.1:c.247C>A	ENSP00000500402.1:p.Pro83Thr
ENST00000356384.4:n.738C>A
ENST00000481739.1:c.328C>A	ENSP00000419692.1:p.Pro110Thr
NM_001291920.1:c.247C>A	NP_001278849.1:p.Pro83Thr
NM_001291921.1:c.37C>A	NP_001278850.1:p.Pro13Thr
NM_002957.5:c.328C>A	NP_002948.1:p.Pro110Thr
NM_002957.6:c.328C>A MANE Select	NP_002948.1:p.Pro110Thr
NM_001291921.2:c.37C>A	NP_001278850.1:p.Pro13Thr
NM_001291920.2:c.247C>A	NP_001278849.1:p.Pro83Thr