Canonical Allele Identifier: CA2147075361

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503448C= , CM000676.2:g.74503448C=	GRCh38
NC_000014.8:g.74970151C= , CM000676.1:g.74970151C=	GRCh37
NC_000014.7:g.74039904C=	NCBI36
NG_021486.1:g.113884G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.4720+21G= MANE Select	ENSP00000261978.4:n.4720+21G=
ENST00000261978.8:c.4720+21G=	ENSP00000261978.4:n.4720+21G=
ENST00000553939.5:c.4720+21G=	ENSP00000452110.1:n.4720+21G=
ENST00000556690.5:c.4588+21G=	ENSP00000451477.1:n.4588+21G=
NM_000428.2:c.4720+21G=	NP_000419.1:n.4720+21G=
XM_011536765.1:c.4339+21G=	XP_011535067.1:n.4339+21G=
XM_011536766.1:c.4261+21G=	XP_011535068.1:n.4261+21G=
XM_011536767.1:c.4237+21G=	XP_011535069.1:n.4237+21G=
XM_011536765.2:c.4339+21G=	XP_011535067.1:n.4339+21G=
NM_000428.3:c.4720+21G= MANE Select	NP_000419.1:n.4720+21G=