Canonical Allele Identifier: CA1205613257

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168291026G= , CM000663.2:g.168291026G=	GRCh38
NC_000001.10:g.168260264G= , CM000663.1:g.168260264G=	GRCh37
NC_000001.9:g.166526888G=	NCBI36
NG_008244.1:g.14987G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.204-134G= MANE Select	ENSP00000356795.3:n.204-134G=
ENST00000367821.7:c.204-134G=	ENSP00000356795.3:n.204-134G=
NM_005149.2:c.204-134G=	NP_005140.1:n.204-134G=
NM_005149.3:c.204-134G= MANE Select	NP_005140.1:n.204-134G=