Canonical Allele Identifier: CA1140767003

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293286T= , CM000663.2:g.168293286T=	GRCh38
NC_000001.10:g.168262524T= , CM000663.1:g.168262524T=	GRCh37
NC_000001.9:g.166529148T=	NCBI36
NG_008244.1:g.17247T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+8T= MANE Select	ENSP00000356795.3:n.603+8T=
ENST00000367821.7:c.603+8T=	ENSP00000356795.3:n.603+8T=
ENST00000431969.5:c.400+8T=
NM_005149.2:c.603+8T=	NP_005140.1:n.603+8T=
NM_005149.3:c.603+8T= MANE Select	NP_005140.1:n.603+8T=