Canonical Allele Identifier: CA2147085119

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74526070C= , CM000676.2:g.74526070C=	GRCh38
NC_000014.8:g.74992773C= , CM000676.1:g.74992773C=	GRCh37
NC_000014.7:g.74062526C=	NCBI36
NG_021486.1:g.91262G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000428.3:c.2428+5G= MANE Select	NP_000419.1:n.2428+5G=
ENST00000261978.9:c.2428+5G= MANE Select	ENSP00000261978.4:n.2428+5G=
NM_000428.2:c.2428+5G=	NP_000419.1:n.2428+5G=
ENST00000261978.8:c.2428+5G=	ENSP00000261978.4:n.2428+5G=
ENST00000553939.5:c.2428+5G=	ENSP00000452110.1:n.2428+5G=
ENST00000556690.5:c.2428+5G=	ENSP00000451477.1:n.2428+5G=
XM_011536765.1:c.2047+5G=	XP_011535067.1:n.2047+5G=
XM_011536765.2:c.2047+5G=	XP_011535067.1:n.2047+5G=
XM_011536766.1:c.1969+5G=	XP_011535068.1:n.1969+5G=
XM_011536767.1:c.1945+5G=	XP_011535069.1:n.1945+5G=