Canonical Allele Identifier: CA201083801
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs919807354
gnomAD v3: 9-134408009-G-A
gnomAD v4: 9-134408009-G-A
MyVariant Identifiers: chr9:g.134408009G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408009G>A , CM000671.2:g.134408009G>A GRCh38
NC_000009.11:g.137299855G>A , CM000671.1:g.137299855G>A GRCh37
NC_000009.10:g.136439676G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.280-140G>A MANE Select ENSP00000419692.1:n.280-140G>A
ENST00000672570.1:c.199-140G>A ENSP00000500402.1:n.199-140G>A
ENST00000356384.4:n.690-140G>A
ENST00000481739.1:c.280-140G>A ENSP00000419692.1:n.280-140G>A
NM_001291920.1:c.199-140G>A NP_001278849.1:n.199-140G>A
NM_001291921.1:c.-12-140G>A NP_001278850.1:n.-12-140G>A
NM_002957.5:c.280-140G>A NP_002948.1:n.280-140G>A
NM_002957.6:c.280-140G>A MANE Select NP_002948.1:n.280-140G>A
NM_001291921.2:c.-12-140G>A NP_001278850.1:n.-12-140G>A
NM_001291920.2:c.199-140G>A NP_001278849.1:n.199-140G>A
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