Canonical Allele Identifier: CA5317709
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs201544640
ExAC: 9:137300045 C / G
gnomAD v2: 9-137300045-C-G
gnomAD v3: 9-134408199-C-G
gnomAD v4: 9-134408199-C-G
MyVariant Identifiers: chr9:g.137300045C>G (hg19) chr9:g.134408199C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408199C>G , CM000671.2:g.134408199C>G GRCh38
NC_000009.11:g.137300045C>G , CM000671.1:g.137300045C>G GRCh37
NC_000009.10:g.136439866C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.330C>G MANE Select ENSP00000419692.1:p.Pro110=
ENST00000672570.1:c.249C>G ENSP00000500402.1:p.Pro83=
ENST00000356384.4:n.740C>G
ENST00000481739.1:c.330C>G ENSP00000419692.1:p.Pro110=
NM_001291920.1:c.249C>G NP_001278849.1:p.Pro83=
NM_001291921.1:c.39C>G NP_001278850.1:p.Pro13=
NM_002957.5:c.330C>G NP_002948.1:p.Pro110=
NM_002957.6:c.330C>G MANE Select NP_002948.1:p.Pro110=
NM_001291921.2:c.39C>G NP_001278850.1:p.Pro13=
NM_001291920.2:c.249C>G NP_001278849.1:p.Pro83=
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