Canonical Allele Identifier: CA2786202907
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375571A>G , CM000671.2:g.134375571A>G GRCh38
NC_000009.11:g.137267417A>G , CM000671.1:g.137267417A>G GRCh37
NC_000009.10:g.136407238A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.29-26061A>G MANE Select ENSP00000419692.1:n.29-26061A>G
ENST00000356384.4:n.293+1441A>G
ENST00000481739.1:c.29-26061A>G ENSP00000419692.1:n.29-26061A>G
ENST00000484822.1:n.453-26061A>G
NM_002957.5:c.29-26061A>G NP_002948.1:n.29-26061A>G
NM_002957.6:c.29-26061A>G MANE Select NP_002948.1:n.29-26061A>G