Canonical Allele Identifier: CA860857837
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1195110331
MyVariant Identifiers: chr9:g.137301798A>C (hg19) chr9:g.134409952A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134409952A>C , CM000671.2:g.134409952A>C GRCh38
NC_000009.11:g.137301798A>C , CM000671.1:g.137301798A>C GRCh37
NC_000009.10:g.136441619A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.610+833A>C MANE Select ENSP00000419692.1:n.610+833A>C
ENST00000672570.1:c.529+833A>C ENSP00000500402.1:n.529+833A>C
ENST00000356384.4:n.1020+833A>C
ENST00000481739.1:c.610+833A>C ENSP00000419692.1:n.610+833A>C
NM_001291920.1:c.529+833A>C NP_001278849.1:n.529+833A>C
NM_001291921.1:c.319+833A>C NP_001278850.1:n.319+833A>C
NM_002957.5:c.610+833A>C NP_002948.1:n.610+833A>C
NM_002957.6:c.610+833A>C MANE Select NP_002948.1:n.610+833A>C
NM_001291921.2:c.319+833A>C NP_001278850.1:n.319+833A>C
NM_001291920.2:c.529+833A>C NP_001278849.1:n.529+833A>C
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