Canonical Allele Identifier: CA2147073491

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74501044A= , CM000676.2:g.74501044A=	GRCh38
NC_000014.8:g.74967747A= , CM000676.1:g.74967747A=	GRCh37
NC_000014.7:g.74037500A=	NCBI36
NG_021486.1:g.116288T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.5321-15T= MANE Select	ENSP00000261978.4:n.5321-15T=
ENST00000261978.8:c.5321-15T=	ENSP00000261978.4:n.5321-15T=
ENST00000553939.5:c.*100-15T=	ENSP00000452110.1:n.*100-15T=
ENST00000554861.1:n.539-15T=
ENST00000556690.5:c.5189-15T=	ENSP00000451477.1:n.5189-15T=
NM_000428.2:c.5321-15T=	NP_000419.1:n.5321-15T=
XM_011536765.1:c.4940-15T=	XP_011535067.1:n.4940-15T=
XM_011536766.1:c.4862-15T=	XP_011535068.1:n.4862-15T=
XM_011536767.1:c.4838-15T=	XP_011535069.1:n.4838-15T=
XM_011536765.2:c.4940-15T=	XP_011535067.1:n.4940-15T=
NM_000428.3:c.5321-15T= MANE Select	NP_000419.1:n.5321-15T=