Canonical Allele Identifier: CA375452691
Gene: RXRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137300128G>C (hg19) chr9:g.134408282G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408282G>C , CM000671.2:g.134408282G>C GRCh38
NC_000009.11:g.137300128G>C , CM000671.1:g.137300128G>C GRCh37
NC_000009.10:g.136439949G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.413G>C MANE Select ENSP00000419692.1:p.Cys138Ser
ENST00000672570.1:c.332G>C ENSP00000500402.1:p.Cys111Ser
ENST00000356384.4:n.823G>C
ENST00000481739.1:c.413G>C ENSP00000419692.1:p.Cys138Ser
NM_001291920.1:c.332G>C NP_001278849.1:p.Cys111Ser
NM_001291921.1:c.122G>C NP_001278850.1:p.Cys41Ser
NM_002957.5:c.413G>C NP_002948.1:p.Cys138Ser
NM_002957.6:c.413G>C MANE Select NP_002948.1:p.Cys138Ser
NM_001291921.2:c.122G>C NP_001278850.1:p.Cys41Ser
NM_001291920.2:c.332G>C NP_001278849.1:p.Cys111Ser
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