Canonical Allele Identifier: CA386869552
Gene: TBX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674746T>A , CM000674.2:g.114674746T>A GRCh38
NC_000012.11:g.115112551T>A , CM000674.1:g.115112551T>A GRCh37
NC_000012.10:g.113596934T>A NCBI36
NG_008315.1:g.14419A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1129A>T MANE Select ENSP00000257567.2:p.Thr377Ser
ENST00000257566.7:c.1189A>T ENSP00000257566.3:p.Thr397Ser
ENST00000349155.6:c.1129A>T ENSP00000257567.2:p.Thr377Ser
ENST00000613550.1:c.1129A>T ENSP00000480048.1:p.Thr377Ser
NM_005996.3:c.1129A>T NP_005987.3:p.Thr377Ser
NM_016569.3:c.1189A>T NP_057653.3:p.Thr397Ser
NM_005996.4:c.1129A>T MANE Select NP_005987.3:p.Thr377Ser
NM_016569.4:c.1189A>T NP_057653.3:p.Thr397Ser