Canonical Allele Identifier: CA5317711

Gene: RXRA

Linked Data

• dbSNP Id: rs764056224
• ExAC: 9:137300046 C / G
• gnomAD v2: 9-137300046-C-G
• gnomAD v4: 9-134408200-C-G
• MyVariant Identifiers: chr9:g.137300046C>G (hg19) ; chr9:g.134408200C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408200C>G , CM000671.2:g.134408200C>G	GRCh38
NC_000009.11:g.137300046C>G , CM000671.1:g.137300046C>G	GRCh37
NC_000009.10:g.136439867C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.331C>G MANE Select	ENSP00000419692.1:p.Leu111Val
ENST00000672570.1:c.250C>G	ENSP00000500402.1:p.Leu84Val
ENST00000356384.4:n.741C>G
ENST00000481739.1:c.331C>G	ENSP00000419692.1:p.Leu111Val
NM_001291920.1:c.250C>G	NP_001278849.1:p.Leu84Val
NM_001291921.1:c.40C>G	NP_001278850.1:p.Leu14Val
NM_002957.5:c.331C>G	NP_002948.1:p.Leu111Val
NM_002957.6:c.331C>G MANE Select	NP_002948.1:p.Leu111Val
NM_001291921.2:c.40C>G	NP_001278850.1:p.Leu14Val
NM_001291920.2:c.250C>G	NP_001278849.1:p.Leu84Val