Canonical Allele Identifier: CA2786202905
Gene: RXRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375569G>T , CM000671.2:g.134375569G>T GRCh38
NC_000009.11:g.137267415G>T , CM000671.1:g.137267415G>T GRCh37
NC_000009.10:g.136407236G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-26063G>T MANE Select ENSP00000419692.1:n.29-26063G>T
ENST00000356384.4:n.293+1439G>T
ENST00000481739.1:c.29-26063G>T ENSP00000419692.1:n.29-26063G>T
ENST00000484822.1:n.453-26063G>T
NM_002957.5:c.29-26063G>T NP_002948.1:n.29-26063G>T
NM_002957.6:c.29-26063G>T MANE Select NP_002948.1:n.29-26063G>T
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