Canonical Allele Identifier: CA2649007504
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293281_168293282del , CM000663.2:g.168293281_168293282del GRCh38
NC_000001.10:g.168262519_168262520del , CM000663.1:g.168262519_168262520del GRCh37
NC_000001.9:g.166529143_166529144del NCBI36
NG_008244.1:g.17242_17243del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+3_603+4del MANE Select ENSP00000356795.3:n.603+3_603+4del
ENST00000367821.7:c.603+3_603+4del ENSP00000356795.3:n.603+3_603+4del
ENST00000431969.5:c.400+3_400+4del
NM_005149.2:c.603+3_603+4del NP_005140.1:n.603+3_603+4del
NM_005149.3:c.603+3_603+4del MANE Select NP_005140.1:n.603+3_603+4del