Canonical Allele Identifier: CA2621128890
Gene: TBX3 HGNC NCBI

Linked Data

gnomAD v4: 12-114670575-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114670575C>T , CM000674.2:g.114670575C>T GRCh38
NC_000012.11:g.115108380C>T , CM000674.1:g.115108380C>T GRCh37
NC_000012.10:g.113592763C>T NCBI36
NG_008315.1:g.18590G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000349155.7:c.*1266G>A MANE Select ENSP00000257567.2:n.*1266G>A
ENST00000257566.7:c.*1266G>A ENSP00000257566.3:n.*1266G>A
ENST00000349155.6:c.*1266G>A ENSP00000257567.2:n.*1266G>A
NM_005996.3:c.*1266G>A NP_005987.3:n.*1266G>A
NM_016569.3:c.*1266G>A NP_057653.3:n.*1266G>A
NM_005996.4:c.*1266G>A MANE Select NP_005987.3:n.*1266G>A
NM_016569.4:c.*1266G>A NP_057653.3:n.*1266G>A
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