Canonical Allele Identifier: CA2147122456

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74611618C= , CM000676.2:g.74611618C=	GRCh38
NC_000014.8:g.75078321C= , CM000676.1:g.75078321C=	GRCh37
NC_000014.7:g.74148074C=	NCBI36
NG_021486.1:g.5714G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261978.9:c.327G= MANE Select	ENSP00000261978.4:p.Ala109=
ENST00000261978.8:c.327G=	ENSP00000261978.4:p.Ala109=
ENST00000553939.5:c.327G=	ENSP00000452110.1:p.Ala109=
ENST00000556690.5:c.327G=	ENSP00000451477.1:p.Ala109=
ENST00000557425.1:n.123+428G=
NM_000428.2:c.327G=	NP_000419.1:p.Ala109=
XM_011536765.1:c.327G=	XP_011535067.1:p.Ala109=
XM_011536767.1:c.11+6966G=	XP_011535069.1:n.11+6966G=
XM_011536765.2:c.327G=	XP_011535067.1:p.Ala109=
NM_000428.3:c.327G= MANE Select	NP_000419.1:p.Ala109=