Canonical Allele Identifier: CA1352164560
Gene: RARB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.25129806T>G , CM000665.2:g.25129806T>G GRCh38
NC_000003.11:g.25171297T>G , CM000665.1:g.25171297T>G GRCh37
NC_000003.10:g.25146301T>G NCBI36
NG_029013.3:g.305484T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000383772.9:c.-327-2355T>G ENSP00000373282.5:n.-327-2355T>G
ENST00000455576.2:c.-279-44313T>G ENSP00000508527.1:n.-279-44313T>G
ENST00000686715.1:c.-279-44313T>G ENSP00000510539.1:n.-279-44313T>G
ENST00000687353.1:c.-279-44313T>G ENSP00000508588.1:n.-279-44313T>G
ENST00000687676.1:c.-279-44313T>G ENSP00000510313.1:n.-279-44313T>G
ENST00000688892.1:c.-279-44313T>G ENSP00000510650.1:n.-279-44313T>G
NM_001290216.2:c.-279-44313T>G NP_001277145.1:n.-279-44313T>G
NM_001290216.3:c.-279-44313T>G NP_001277145.1:n.-279-44313T>G
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