Canonical Allele Identifier: CA1883147335
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1830281521
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134356221G>A , CM000671.2:g.134356221G>A GRCh38
NC_000009.11:g.137248067G>A , CM000671.1:g.137248067G>A GRCh37
NC_000009.10:g.136387888G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.28+29562G>A MANE Select ENSP00000419692.1:n.28+29562G>A
ENST00000481739.1:c.28+29562G>A ENSP00000419692.1:n.28+29562G>A
ENST00000484822.1:n.452+36737G>A
NM_002957.5:c.28+29562G>A NP_002948.1:n.28+29562G>A
NM_002957.6:c.28+29562G>A MANE Select NP_002948.1:n.28+29562G>A
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