Canonical Allele Identifier: CA2147084254

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74524043A= , CM000676.2:g.74524043A=	GRCh38
NC_000014.8:g.74990746A= , CM000676.1:g.74990746A=	GRCh37
NC_000014.7:g.74060499A=	NCBI36
NG_021486.1:g.93289T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000428.3:c.2530+1081T= MANE Select	NP_000419.1:n.2530+1081T=
ENST00000261978.9:c.2530+1081T= MANE Select	ENSP00000261978.4:n.2530+1081T=
NM_000428.2:c.2530+1081T=	NP_000419.1:n.2530+1081T=
ENST00000261978.8:c.2530+1081T=	ENSP00000261978.4:n.2530+1081T=
ENST00000553939.5:c.2530+1081T=	ENSP00000452110.1:n.2530+1081T=
ENST00000556690.5:c.2530+1081T=	ENSP00000451477.1:n.2530+1081T=
XM_011536765.1:c.2149+1081T=	XP_011535067.1:n.2149+1081T=
XM_011536765.2:c.2149+1081T=	XP_011535067.1:n.2149+1081T=
XM_011536766.1:c.2071+1081T=	XP_011535068.1:n.2071+1081T=
XM_011536767.1:c.2047+1081T=	XP_011535069.1:n.2047+1081T=