Canonical Allele Identifier: CA2649007556
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293324_168293325insTT , CM000663.2:g.168293324_168293325insTT GRCh38
NC_000001.10:g.168262562_168262563insTT , CM000663.1:g.168262562_168262563insTT GRCh37
NC_000001.9:g.166529186_166529187insTT NCBI36
NG_008244.1:g.17285_17286insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+46_603+47insTT MANE Select ENSP00000356795.3:n.603+46_603+47insTT
ENST00000367821.7:c.603+46_603+47insTT ENSP00000356795.3:n.603+46_603+47insTT
ENST00000431969.5:c.400+46_400+47insTT
NM_005149.2:c.603+46_603+47insTT NP_005140.1:n.603+46_603+47insTT
NM_005149.3:c.603+46_603+47insTT MANE Select NP_005140.1:n.603+46_603+47insTT