Canonical Allele Identifier: CA2692438846
Gene: RXRA HGNC NCBI

Linked Data

gnomAD v4: 9-134432117-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134432117T>C , CM000671.2:g.134432117T>C GRCh38
NC_000009.11:g.137323963T>C , CM000671.1:g.137323963T>C GRCh37
NC_000009.10:g.136463784T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.1135+121T>C MANE Select ENSP00000419692.1:n.1135+121T>C
ENST00000672570.1:c.1054+121T>C ENSP00000500402.1:n.1054+121T>C
ENST00000356384.4:n.1545+121T>C
ENST00000481739.1:c.1135+121T>C ENSP00000419692.1:n.1135+121T>C
NM_001291920.1:c.1054+121T>C NP_001278849.1:n.1054+121T>C
NM_001291921.1:c.844+121T>C NP_001278850.1:n.844+121T>C
NM_002957.5:c.1135+121T>C NP_002948.1:n.1135+121T>C
NM_002957.6:c.1135+121T>C MANE Select NP_002948.1:n.1135+121T>C
NM_001291921.2:c.844+121T>C NP_001278850.1:n.844+121T>C
NM_001291920.2:c.1054+121T>C NP_001278849.1:n.1054+121T>C
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