Canonical Allele Identifier: CA1205614351

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293593G= , CM000663.2:g.168293593G=	GRCh38
NC_000001.10:g.168262831G= , CM000663.1:g.168262831G=	GRCh37
NC_000001.9:g.166529455G=	NCBI36
NG_008244.1:g.17554G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+315G= MANE Select	ENSP00000356795.3:n.603+315G=
ENST00000367821.7:c.603+315G=	ENSP00000356795.3:n.603+315G=
ENST00000431969.5:c.400+315G=
NM_005149.2:c.603+315G=	NP_005140.1:n.603+315G=
NM_005149.3:c.603+315G= MANE Select	NP_005140.1:n.603+315G=