Canonical Allele Identifier: CA2574084067
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293309_168293310insAG , CM000663.2:g.168293309_168293310insAG GRCh38
NC_000001.10:g.168262547_168262548insAG , CM000663.1:g.168262547_168262548insAG GRCh37
NC_000001.9:g.166529171_166529172insAG NCBI36
NG_008244.1:g.17270_17271insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+31_603+32insAG MANE Select ENSP00000356795.3:n.603+31_603+32insAG
ENST00000367821.7:c.603+31_603+32insAG ENSP00000356795.3:n.603+31_603+32insAG
ENST00000431969.5:c.400+31_400+32insAG
NM_005149.2:c.603+31_603+32insAG NP_005140.1:n.603+31_603+32insAG
NM_005149.3:c.603+31_603+32insAG MANE Select NP_005140.1:n.603+31_603+32insAG