Canonical Allele Identifier: CA860844235
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1370436048
gnomAD v3: 9-134375689-G-T
gnomAD v4: 9-134375689-G-T
MyVariant Identifiers: chr9:g.137267535G>T (hg19) chr9:g.134375689G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375689G>T , CM000671.2:g.134375689G>T GRCh38
NC_000009.11:g.137267535G>T , CM000671.1:g.137267535G>T GRCh37
NC_000009.10:g.136407356G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.29-25943G>T MANE Select ENSP00000419692.1:n.29-25943G>T
ENST00000356384.4:n.293+1559G>T
ENST00000481739.1:c.29-25943G>T ENSP00000419692.1:n.29-25943G>T
ENST00000484822.1:n.453-25943G>T
NM_002957.5:c.29-25943G>T NP_002948.1:n.29-25943G>T
NM_002957.6:c.29-25943G>T MANE Select NP_002948.1:n.29-25943G>T
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