Canonical Allele Identifier: CA1205614172

Gene: TBX19

Linked Data

• dbSNP Id: rs1553289048

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293284_168293291del , CM000663.2:g.168293284_168293291del	GRCh38
NC_000001.10:g.168262522_168262529del , CM000663.1:g.168262522_168262529del	GRCh37
NC_000001.9:g.166529146_166529153del	NCBI36
NG_008244.1:g.17245_17252del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+6_603+13del MANE Select	ENSP00000356795.3:n.603+6_603+13del
ENST00000367821.7:c.603+6_603+13del	ENSP00000356795.3:n.603+6_603+13del
ENST00000431969.5:c.400+6_400+13del
NM_005149.2:c.603+6_603+13del	NP_005140.1:n.603+6_603+13del
NM_005149.3:c.603+6_603+13del MANE Select	NP_005140.1:n.603+6_603+13del