Canonical Allele Identifier: CA645520095
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293287_168293288insGTT , CM000663.2:g.168293287_168293288insGTT GRCh38
NC_000001.10:g.168262525_168262526insGTT , CM000663.1:g.168262525_168262526insGTT GRCh37
NC_000001.9:g.166529149_166529150insGTT NCBI36
NG_008244.1:g.17248_17249insGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+9_603+10insGTT MANE Select ENSP00000356795.3:n.603+9_603+10insGTT
ENST00000367821.7:c.603+9_603+10insGTT ENSP00000356795.3:n.603+9_603+10insGTT
ENST00000431969.5:c.400+9_400+10insGTT
NM_005149.2:c.603+9_603+10insGTT NP_005140.1:n.603+9_603+10insGTT
NM_005149.3:c.603+9_603+10insGTT MANE Select NP_005140.1:n.603+9_603+10insGTT