Canonical Allele Identifier: CA2649007553

Gene: TBX19

Linked Data

• gnomAD v4: 1-168293320-T-TGTGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293321_168293325dup , CM000663.2:g.168293321_168293325dup	GRCh38
NC_000001.10:g.168262559_168262563dup , CM000663.1:g.168262559_168262563dup	GRCh37
NC_000001.9:g.166529183_166529187dup	NCBI36
NG_008244.1:g.17282_17286dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+43_603+47dup MANE Select	ENSP00000356795.3:n.603+43_603+47dup
ENST00000367821.7:c.603+43_603+47dup	ENSP00000356795.3:n.603+43_603+47dup
ENST00000431969.5:c.400+43_400+47dup
NM_005149.2:c.603+43_603+47dup	NP_005140.1:n.603+43_603+47dup
NM_005149.3:c.603+43_603+47dup MANE Select	NP_005140.1:n.603+43_603+47dup