Canonical Allele Identifier: CA2649007307
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291103_168291105del , CM000663.2:g.168291103_168291105del GRCh38
NC_000001.10:g.168260341_168260343del , CM000663.1:g.168260341_168260343del GRCh37
NC_000001.9:g.166526965_166526967del NCBI36
NG_008244.1:g.15064_15066del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.204-57_204-55del MANE Select ENSP00000356795.3:n.204-57_204-55del
ENST00000367821.7:c.204-57_204-55del ENSP00000356795.3:n.204-57_204-55del
NM_005149.2:c.204-57_204-55del NP_005140.1:n.204-57_204-55del
NM_005149.3:c.204-57_204-55del MANE Select NP_005140.1:n.204-57_204-55del