Canonical Allele Identifier: CA2649007543
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293309del , CM000663.2:g.168293309del GRCh38
NC_000001.10:g.168262547del , CM000663.1:g.168262547del GRCh37
NC_000001.9:g.166529171del NCBI36
NG_008244.1:g.17270del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+31del MANE Select ENSP00000356795.3:n.603+31del
ENST00000367821.7:c.603+31del ENSP00000356795.3:n.603+31del
ENST00000431969.5:c.400+31del
NM_005149.2:c.603+31del NP_005140.1:n.603+31del
NM_005149.3:c.603+31del MANE Select NP_005140.1:n.603+31del