Canonical Allele Identifier: CA12974931
Gene: RXRA HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.134437460G>A
GRCh37 chr9:g.137329306G>A
gnomAD v2:
9:137329306 G / A
gnomAD v3:
9:134437460 G / A
gnomAD v4:
chr9-134437460-G-A
Joint Max Group AF 0.64992378 (NFE)
Genomes Max Group AF 0.64969615 (NFE)
Exomes Max Group AF 0.62584395 (NFE)
dbSNP:
4240711
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134437460G>A , CM000671.2:g.134437460G>A GRCh38
NC_000009.11:g.137329306G>A , CM000671.1:g.137329306G>A GRCh37
NC_000009.10:g.136469127G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.*846G>A MANE Select ENSP00000419692.1:n.*846G>A
ENST00000356384.4:n.2645G>A
NM_001291920.1:c.*846G>A NP_001278849.1:n.*846G>A
NM_001291921.1:c.*846G>A NP_001278850.1:n.*846G>A
NM_002957.5:c.*846G>A NP_002948.1:n.*846G>A
NM_002957.6:c.*846G>A MANE Select NP_002948.1:n.*846G>A
NM_001291921.2:c.*846G>A NP_001278850.1:n.*846G>A
NM_001291920.2:c.*846G>A NP_001278849.1:n.*846G>A
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