Canonical Allele Identifier: CA2147077122

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74508727C= , CM000676.2:g.74508727C=	GRCh38
NC_000014.8:g.74975430C= , CM000676.1:g.74975430C=	GRCh37
NC_000014.7:g.74045183C=	NCBI36
NG_021486.1:g.108605G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000428.3:c.3529G= MANE Select	NP_000419.1:p.Val1177=
ENST00000261978.9:c.3529G= MANE Select	ENSP00000261978.4:p.Val1177=
NM_000428.2:c.3529G=	NP_000419.1:p.Val1177=
ENST00000261978.8:c.3529G=	ENSP00000261978.4:p.Val1177=
ENST00000553939.5:c.3529G=	ENSP00000452110.1:p.Val1177=
ENST00000556206.1:c.326G=
ENST00000556690.5:c.3529G=	ENSP00000451477.1:p.Val1177=
XM_011536765.1:c.3148G=	XP_011535067.1:p.Val1050=
XM_011536765.2:c.3148G=	XP_011535067.1:p.Val1050=
XM_011536766.1:c.3070G=	XP_011535068.1:p.Val1024=
XM_011536767.1:c.3046G=	XP_011535069.1:p.Val1016=