Canonical Allele Identifier: CA1883177688
Gene: RXRA HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134409950A= , CM000671.2:g.134409950A= GRCh38
NC_000009.11:g.137301796A= , CM000671.1:g.137301796A= GRCh37
NC_000009.10:g.136441617A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.610+831A= MANE Select ENSP00000419692.1:n.610+831A=
ENST00000672570.1:c.529+831A= ENSP00000500402.1:n.529+831A=
ENST00000356384.4:n.1020+831A=
ENST00000481739.1:c.610+831A= ENSP00000419692.1:n.610+831A=
NM_001291920.1:c.529+831A= NP_001278849.1:n.529+831A=
NM_001291921.1:c.319+831A= NP_001278850.1:n.319+831A=
NM_002957.5:c.610+831A= NP_002948.1:n.610+831A=
NM_002957.6:c.610+831A= MANE Select NP_002948.1:n.610+831A=
NM_001291921.2:c.319+831A= NP_001278850.1:n.319+831A=
NM_001291920.2:c.529+831A= NP_001278849.1:n.529+831A=
Search 100 bp 5'
Search 100 bp 3'