Canonical Allele Identifier: CA2649007539
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293307_168293308insCG , CM000663.2:g.168293307_168293308insCG GRCh38
NC_000001.10:g.168262545_168262546insCG , CM000663.1:g.168262545_168262546insCG GRCh37
NC_000001.9:g.166529169_166529170insCG NCBI36
NG_008244.1:g.17268_17269insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+29_603+30insCG MANE Select ENSP00000356795.3:n.603+29_603+30insCG
ENST00000367821.7:c.603+29_603+30insCG ENSP00000356795.3:n.603+29_603+30insCG
ENST00000431969.5:c.400+29_400+30insCG
NM_005149.2:c.603+29_603+30insCG NP_005140.1:n.603+29_603+30insCG
NM_005149.3:c.603+29_603+30insCG MANE Select NP_005140.1:n.603+29_603+30insCG