Canonical Allele Identifier: CA1205614249

Gene: TBX19

Linked Data

• dbSNP Id: rs1558191163

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293359_168293360insT , CM000663.2:g.168293359_168293360insT	GRCh38
NC_000001.10:g.168262597_168262598insT , CM000663.1:g.168262597_168262598insT	GRCh37
NC_000001.9:g.166529221_166529222insT	NCBI36
NG_008244.1:g.17320_17321insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+81_603+82insT MANE Select	ENSP00000356795.3:n.603+81_603+82insT
ENST00000367821.7:c.603+81_603+82insT	ENSP00000356795.3:n.603+81_603+82insT
ENST00000431969.5:c.400+81_400+82insT
NM_005149.2:c.603+81_603+82insT	NP_005140.1:n.603+81_603+82insT
NM_005149.3:c.603+81_603+82insT MANE Select	NP_005140.1:n.603+81_603+82insT