Canonical Allele Identifier: CA263588732

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74585971C>T , CM000676.2:g.74585971C>T	GRCh38
NC_000014.8:g.75052674C>T , CM000676.1:g.75052674C>T	GRCh37
NC_000014.7:g.74122427C>T	NCBI36
NG_021486.1:g.31361G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000428.3:c.713G>A MANE Select	NP_000419.1:p.Arg238His
ENST00000261978.9:c.713G>A MANE Select	ENSP00000261978.4:p.Arg238His
NM_000428.2:c.713G>A	NP_000419.1:p.Arg238His
ENST00000261978.8:c.713G>A	ENSP00000261978.4:p.Arg238His
ENST00000553939.5:c.713G>A	ENSP00000452110.1:p.Arg238His
ENST00000556690.5:c.713G>A	ENSP00000451477.1:p.Arg238His
ENST00000557425.1:n.123+26075G>A
XM_011536765.1:c.713G>A	XP_011535067.1:p.Arg238His
XM_011536765.2:c.713G>A	XP_011535067.1:p.Arg238His
XM_011536766.1:c.254G>A	XP_011535068.1:p.Arg85His
XM_011536767.1:c.230G>A	XP_011535069.1:p.Arg77His