Canonical Allele Identifier: CA13021841
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs10881583

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375593T>C , CM000671.2:g.134375593T>C GRCh38
NC_000009.11:g.137267439T>C , CM000671.1:g.137267439T>C GRCh37
NC_000009.10:g.136407260T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-26039T>C MANE Select ENSP00000419692.1:n.29-26039T>C
ENST00000356384.4:n.293+1463T>C
ENST00000481739.1:c.29-26039T>C ENSP00000419692.1:n.29-26039T>C
ENST00000484822.1:n.453-26039T>C
NM_002957.5:c.29-26039T>C NP_002948.1:n.29-26039T>C
NM_002957.6:c.29-26039T>C MANE Select NP_002948.1:n.29-26039T>C