Canonical Allele Identifier: CA2692438878
Gene: RXRA HGNC NCBI

Linked Data

gnomAD v4: 9-134432135-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134432135C>A , CM000671.2:g.134432135C>A GRCh38
NC_000009.11:g.137323981C>A , CM000671.1:g.137323981C>A GRCh37
NC_000009.10:g.136463802C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.1135+139C>A MANE Select ENSP00000419692.1:n.1135+139C>A
ENST00000672570.1:c.1054+139C>A ENSP00000500402.1:n.1054+139C>A
ENST00000356384.4:n.1545+139C>A
ENST00000481739.1:c.1135+139C>A ENSP00000419692.1:n.1135+139C>A
NM_001291920.1:c.1054+139C>A NP_001278849.1:n.1054+139C>A
NM_001291921.1:c.844+139C>A NP_001278850.1:n.844+139C>A
NM_002957.5:c.1135+139C>A NP_002948.1:n.1135+139C>A
NM_002957.6:c.1135+139C>A MANE Select NP_002948.1:n.1135+139C>A
NM_001291921.2:c.844+139C>A NP_001278850.1:n.844+139C>A
NM_001291920.2:c.1054+139C>A NP_001278849.1:n.1054+139C>A
Search 100 bp 5'
Search 100 bp 3'