Canonical Allele Identifier: CA1144120416

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168291217C= , CM000663.2:g.168291217C=	GRCh38
NC_000001.10:g.168260455C= , CM000663.1:g.168260455C=	GRCh37
NC_000001.9:g.166527079C=	NCBI36
NG_008244.1:g.15178C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367821.8:c.261C= MANE Select	ENSP00000356795.3:p.Tyr87=
ENST00000367821.7:c.261C=	ENSP00000356795.3:p.Tyr87=
ENST00000431969.5:c.58C=
NM_005149.2:c.261C=	NP_005140.1:p.Tyr87=
NM_005149.3:c.261C= MANE Select	NP_005140.1:p.Tyr87=