Canonical Allele Identifier: CA1883176847
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1831091330
gnomAD v4: 9-134408338-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408338G>T , CM000671.2:g.134408338G>T GRCh38
NC_000009.11:g.137300184G>T , CM000671.1:g.137300184G>T GRCh37
NC_000009.10:g.136440005G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.430+39G>T MANE Select ENSP00000419692.1:n.430+39G>T
ENST00000672570.1:c.349+39G>T ENSP00000500402.1:n.349+39G>T
ENST00000356384.4:n.840+39G>T
ENST00000481739.1:c.430+39G>T ENSP00000419692.1:n.430+39G>T
NM_001291920.1:c.349+39G>T NP_001278849.1:n.349+39G>T
NM_001291921.1:c.139+39G>T NP_001278850.1:n.139+39G>T
NM_002957.5:c.430+39G>T NP_002948.1:n.430+39G>T
NM_002957.6:c.430+39G>T MANE Select NP_002948.1:n.430+39G>T
NM_001291921.2:c.139+39G>T NP_001278850.1:n.139+39G>T
NM_001291920.2:c.349+39G>T NP_001278849.1:n.349+39G>T
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