Canonical Allele Identifier: CA201032365
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs530404116
gnomAD v2: 9-137248121-G-A
gnomAD v3: 9-134356275-G-A
gnomAD v4: 9-134356275-G-A
MyVariant Identifiers: chr9:g.137248121G>A (hg19) chr9:g.134356275G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134356275G>A , CM000671.2:g.134356275G>A GRCh38
NC_000009.11:g.137248121G>A , CM000671.1:g.137248121G>A GRCh37
NC_000009.10:g.136387942G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.28+29616G>A MANE Select ENSP00000419692.1:n.28+29616G>A
ENST00000481739.1:c.28+29616G>A ENSP00000419692.1:n.28+29616G>A
ENST00000484822.1:n.452+36791G>A
NM_002957.5:c.28+29616G>A NP_002948.1:n.28+29616G>A
NM_002957.6:c.28+29616G>A MANE Select NP_002948.1:n.28+29616G>A
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