Canonical Allele Identifier: CA1205614084
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293041_168293044delinsGGGT , CM000663.2:g.168293041_168293044delinsGGGT GRCh38
NC_000001.10:g.168262279_168262282delinsGGGT , CM000663.1:g.168262279_168262282delinsGGGT GRCh37
NC_000001.9:g.166528903_166528906delinsGGGT NCBI36
NG_008244.1:g.17002_17005delinsGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.469-103_469-100delinsGGGT MANE Select ENSP00000356795.3:n.469-103_469-100delinsGGGT
ENST00000367821.7:c.469-103_469-100delinsGGGT ENSP00000356795.3:n.469-103_469-100delinsGGGT
ENST00000431969.5:c.266-103_266-100delinsGGGT
NM_005149.2:c.469-103_469-100delinsGGGT NP_005140.1:n.469-103_469-100delinsGGGT
NM_005149.3:c.469-103_469-100delinsGGGT MANE Select NP_005140.1:n.469-103_469-100delinsGGGT