Canonical Allele Identifier: CA2147096060

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74551266C= , CM000676.2:g.74551266C=	GRCh38
NC_000014.8:g.75017969C= , CM000676.1:g.75017969C=	GRCh37
NC_000014.7:g.74087722C=	NCBI36
NG_021486.1:g.66066G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.1484G= MANE Select	ENSP00000261978.4:p.Arg495=
ENST00000261978.8:c.1484G=	ENSP00000261978.4:p.Arg495=
ENST00000553939.5:c.1484G=	ENSP00000452110.1:p.Arg495=
ENST00000556690.5:c.1484G=	ENSP00000451477.1:p.Arg495=
ENST00000557425.1:n.208G=
NM_000428.2:c.1484G=	NP_000419.1:p.Arg495=
XM_011536765.1:c.1484G=	XP_011535067.1:p.Arg495=
XM_011536766.1:c.1025G=	XP_011535068.1:p.Arg342=
XM_011536767.1:c.1001G=	XP_011535069.1:p.Arg334=
XM_011536765.2:c.1484G=	XP_011535067.1:p.Arg495=
NM_000428.3:c.1484G= MANE Select	NP_000419.1:p.Arg495=