Canonical Allele Identifier: CA1205613324

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168291220C= , CM000663.2:g.168291220C=	GRCh38
NC_000001.10:g.168260458C= , CM000663.1:g.168260458C=	GRCh37
NC_000001.9:g.166527082C=	NCBI36
NG_008244.1:g.15181C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367821.8:c.264C= MANE Select	ENSP00000356795.3:p.Ser88=
ENST00000367821.7:c.264C=	ENSP00000356795.3:p.Ser88=
ENST00000431969.5:c.61C=
NM_005149.2:c.264C=	NP_005140.1:p.Ser88=
NM_005149.3:c.264C= MANE Select	NP_005140.1:p.Ser88=