Canonical Allele Identifier: CA2831176110

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293327_168293328insT , CM000663.2:g.168293327_168293328insT	GRCh38
NC_000001.10:g.168262565_168262566insT , CM000663.1:g.168262565_168262566insT	GRCh37
NC_000001.9:g.166529189_166529190insT	NCBI36
NG_008244.1:g.17288_17289insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+49_603+50insT MANE Select	ENSP00000356795.3:n.603+49_603+50insT
ENST00000367821.7:c.603+49_603+50insT	ENSP00000356795.3:n.603+49_603+50insT
ENST00000431969.5:c.400+49_400+50insT
NM_005149.2:c.603+49_603+50insT	NP_005140.1:n.603+49_603+50insT
NM_005149.3:c.603+49_603+50insT MANE Select	NP_005140.1:n.603+49_603+50insT