Canonical Allele Identifier: CA482136159
Gene: TBX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.115112483A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674678A>C , CM000674.2:g.114674678A>C GRCh38
NC_000012.11:g.115112483A>C , CM000674.1:g.115112483A>C GRCh37
NC_000012.10:g.113596866A>C NCBI36
NG_008315.1:g.14487T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000349155.7:c.1197T>G MANE Select ENSP00000257567.2:p.Ala399=
ENST00000257566.7:c.1257T>G ENSP00000257566.3:p.Ala419=
ENST00000349155.6:c.1197T>G ENSP00000257567.2:p.Ala399=
ENST00000613550.1:c.1197T>G ENSP00000480048.1:p.Ala399=
NM_005996.3:c.1197T>G NP_005987.3:p.Ala399=
NM_016569.3:c.1257T>G NP_057653.3:p.Ala419=
NM_005996.4:c.1197T>G MANE Select NP_005987.3:p.Ala399=
NM_016569.4:c.1257T>G NP_057653.3:p.Ala419=
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