Canonical Allele Identifier: CA487155764

Gene: LTBP2

Linked Data

• MyVariant Identifiers: chr14:g.74967680A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74500977A>T , CM000676.2:g.74500977A>T	GRCh38
NC_000014.8:g.74967680A>T , CM000676.1:g.74967680A>T	GRCh37
NC_000014.7:g.74037433A>T	NCBI36
NG_021486.1:g.116355T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261978.9:c.5373T>A MANE Select	ENSP00000261978.4:p.Gly1791=
ENST00000261978.8:c.5373T>A	ENSP00000261978.4:p.Gly1791=
ENST00000553939.5:c.*152T>A	ENSP00000452110.1:n.*152T>A
ENST00000554861.1:n.591T>A
ENST00000556690.5:c.5241T>A	ENSP00000451477.1:p.Gly1747=
NM_000428.2:c.5373T>A	NP_000419.1:p.Gly1791=
XM_011536765.1:c.4992T>A	XP_011535067.1:p.Gly1664=
XM_011536766.1:c.4914T>A	XP_011535068.1:p.Gly1638=
XM_011536767.1:c.4890T>A	XP_011535069.1:p.Gly1630=
XM_011536765.2:c.4992T>A	XP_011535067.1:p.Gly1664=
NM_000428.3:c.5373T>A MANE Select	NP_000419.1:p.Gly1791=