Canonical Allele Identifier: CA375452638
Gene: RXRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137300118T>A (hg19) chr9:g.134408272T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408272T>A , CM000671.2:g.134408272T>A GRCh38
NC_000009.11:g.137300118T>A , CM000671.1:g.137300118T>A GRCh37
NC_000009.10:g.136439939T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.403T>A MANE Select ENSP00000419692.1:p.Cys135Ser
ENST00000672570.1:c.322T>A ENSP00000500402.1:p.Cys108Ser
ENST00000356384.4:n.813T>A
ENST00000481739.1:c.403T>A ENSP00000419692.1:p.Cys135Ser
NM_001291920.1:c.322T>A NP_001278849.1:p.Cys108Ser
NM_001291921.1:c.112T>A NP_001278850.1:p.Cys38Ser
NM_002957.5:c.403T>A NP_002948.1:p.Cys135Ser
NM_002957.6:c.403T>A MANE Select NP_002948.1:p.Cys135Ser
NM_001291921.2:c.112T>A NP_001278850.1:p.Cys38Ser
NM_001291920.2:c.322T>A NP_001278849.1:p.Cys108Ser
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