Canonical Allele Identifier: CA2574084062
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293283_168293284insTGTGTG , CM000663.2:g.168293283_168293284insTGTGTG GRCh38
NC_000001.10:g.168262521_168262522insTGTGTG , CM000663.1:g.168262521_168262522insTGTGTG GRCh37
NC_000001.9:g.166529145_166529146insTGTGTG NCBI36
NG_008244.1:g.17244_17245insTGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+5_603+6insTGTGTG MANE Select ENSP00000356795.3:n.603+5_603+6insTGTGTG
ENST00000367821.7:c.603+5_603+6insTGTGTG ENSP00000356795.3:n.603+5_603+6insTGTGTG
ENST00000431969.5:c.400+5_400+6insTGTGTG
NM_005149.2:c.603+5_603+6insTGTGTG NP_005140.1:n.603+5_603+6insTGTGTG
NM_005149.3:c.603+5_603+6insTGTGTG MANE Select NP_005140.1:n.603+5_603+6insTGTGTG