Canonical Allele Identifier: CA919180475
Gene: TBX3 HGNC NCBI

Linked Data

dbSNP Id: rs143862488

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674942dup , CM000674.2:g.114674942dup GRCh38
NC_000012.11:g.115112747dup , CM000674.1:g.115112747dup GRCh37
NC_000012.10:g.113597130dup NCBI36
NG_008315.1:g.14223dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1040-107dup MANE Select ENSP00000257567.2:n.1040-107dup
ENST00000257566.7:c.1100-107dup ENSP00000257566.3:n.1100-107dup
ENST00000349155.6:c.1040-107dup ENSP00000257567.2:n.1040-107dup
ENST00000613550.1:c.1040-107dup ENSP00000480048.1:n.1040-107dup
NM_005996.3:c.1040-107dup NP_005987.3:n.1040-107dup
NM_016569.3:c.1100-107dup NP_057653.3:n.1100-107dup
NM_005996.4:c.1040-107dup MANE Select NP_005987.3:n.1040-107dup
NM_016569.4:c.1100-107dup NP_057653.3:n.1100-107dup