Canonical Allele Identifier: CA467648642
Gene: RXRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137300063C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408217C>A , CM000671.2:g.134408217C>A GRCh38
NC_000009.11:g.137300063C>A , CM000671.1:g.137300063C>A GRCh37
NC_000009.10:g.136439884C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.348C>A MANE Select ENSP00000419692.1:p.Val116=
ENST00000672570.1:c.267C>A ENSP00000500402.1:p.Val89=
ENST00000356384.4:n.758C>A
ENST00000481739.1:c.348C>A ENSP00000419692.1:p.Val116=
NM_001291920.1:c.267C>A NP_001278849.1:p.Val89=
NM_001291921.1:c.57C>A NP_001278850.1:p.Val19=
NM_002957.5:c.348C>A NP_002948.1:p.Val116=
NM_002957.6:c.348C>A MANE Select NP_002948.1:p.Val116=
NM_001291921.2:c.57C>A NP_001278850.1:p.Val19=
NM_001291920.2:c.267C>A NP_001278849.1:p.Val89=