Canonical Allele Identifier: CA375452561
Gene: RXRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137300101C>A (hg19) chr9:g.134408255C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408255C>A , CM000671.2:g.134408255C>A GRCh38
NC_000009.11:g.137300101C>A , CM000671.1:g.137300101C>A GRCh37
NC_000009.10:g.136439922C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.386C>A MANE Select ENSP00000419692.1:p.Ser129Tyr
ENST00000672570.1:c.305C>A ENSP00000500402.1:p.Ser102Tyr
ENST00000356384.4:n.796C>A
ENST00000481739.1:c.386C>A ENSP00000419692.1:p.Ser129Tyr
NM_001291920.1:c.305C>A NP_001278849.1:p.Ser102Tyr
NM_001291921.1:c.95C>A NP_001278850.1:p.Ser32Tyr
NM_002957.5:c.386C>A NP_002948.1:p.Ser129Tyr
NM_002957.6:c.386C>A MANE Select NP_002948.1:p.Ser129Tyr
NM_001291921.2:c.95C>A NP_001278850.1:p.Ser32Tyr
NM_001291920.2:c.305C>A NP_001278849.1:p.Ser102Tyr
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