Canonical Allele Identifier: CA1883155511
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1830546590

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375627dup , CM000671.2:g.134375627dup GRCh38
NC_000009.11:g.137267473dup , CM000671.1:g.137267473dup GRCh37
NC_000009.10:g.136407294dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-26005dup MANE Select ENSP00000419692.1:n.29-26005dup
ENST00000356384.4:n.293+1497dup
ENST00000481739.1:c.29-26005dup ENSP00000419692.1:n.29-26005dup
ENST00000484822.1:n.453-26005dup
NM_002957.5:c.29-26005dup NP_002948.1:n.29-26005dup
NM_002957.6:c.29-26005dup MANE Select NP_002948.1:n.29-26005dup