Canonical Allele Identifier: CA375451931
Gene: RXRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137300000C>G (hg19) chr9:g.134408154C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408154C>G , CM000671.2:g.134408154C>G GRCh38
NC_000009.11:g.137300000C>G , CM000671.1:g.137300000C>G GRCh37
NC_000009.10:g.136439821C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.285C>G MANE Select ENSP00000419692.1:p.Ser95Arg
ENST00000672570.1:c.204C>G ENSP00000500402.1:p.Ser68Arg
ENST00000356384.4:n.695C>G
ENST00000481739.1:c.285C>G ENSP00000419692.1:p.Ser95Arg
NM_001291920.1:c.204C>G NP_001278849.1:p.Ser68Arg
NM_001291921.1:c.-7C>G NP_001278850.1:n.-7C>G
NM_002957.5:c.285C>G NP_002948.1:p.Ser95Arg
NM_002957.6:c.285C>G MANE Select NP_002948.1:p.Ser95Arg
NM_001291921.2:c.-7C>G NP_001278850.1:n.-7C>G
NM_001291920.2:c.204C>G NP_001278849.1:p.Ser68Arg
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