Canonical Allele Identifier: CA860844229
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1423594788
gnomAD v3: 9-134375621-C-CGGGCCA
gnomAD v4: 9-134375621-C-CGGGCCA
MyVariant Identifiers: chr9:g.137267467_137267468insGGGCCA (hg19) chr9:g.134375621_134375622insGGGCCA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375629_134375634dup , CM000671.2:g.134375629_134375634dup GRCh38
NC_000009.11:g.137267475_137267480dup , CM000671.1:g.137267475_137267480dup GRCh37
NC_000009.10:g.136407296_136407301dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-26003_29-25998dup MANE Select ENSP00000419692.1:n.29-26003_29-25998dup
ENST00000356384.4:n.293+1499_293+1504dup
ENST00000481739.1:c.29-26003_29-25998dup ENSP00000419692.1:n.29-26003_29-25998dup
ENST00000484822.1:n.453-26003_453-25998dup
NM_002957.5:c.29-26003_29-25998dup NP_002948.1:n.29-26003_29-25998dup
NM_002957.6:c.29-26003_29-25998dup MANE Select NP_002948.1:n.29-26003_29-25998dup
Search 100 bp 5'
Search 100 bp 3'