Canonical Allele Identifier: CA390381979

Gene: LTBP2

Linked Data

• MyVariant Identifiers: chr14:g.74967663T>A (hg19) ; chr14:g.74500960T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74500960T>A , CM000676.2:g.74500960T>A	GRCh38
NC_000014.8:g.74967663T>A , CM000676.1:g.74967663T>A	GRCh37
NC_000014.7:g.74037416T>A	NCBI36
NG_021486.1:g.116372A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.5390A>T MANE Select	ENSP00000261978.4:p.Glu1797Val
ENST00000261978.8:c.5390A>T	ENSP00000261978.4:p.Glu1797Val
ENST00000553939.5:c.*169A>T	ENSP00000452110.1:n.*169A>T
ENST00000554861.1:n.608A>T
ENST00000556690.5:c.5258A>T	ENSP00000451477.1:p.Glu1753Val
NM_000428.2:c.5390A>T	NP_000419.1:p.Glu1797Val
XM_011536765.1:c.5009A>T	XP_011535067.1:p.Glu1670Val
XM_011536766.1:c.4931A>T	XP_011535068.1:p.Glu1644Val
XM_011536767.1:c.4907A>T	XP_011535069.1:p.Glu1636Val
XM_011536765.2:c.5009A>T	XP_011535067.1:p.Glu1670Val
NM_000428.3:c.5390A>T MANE Select	NP_000419.1:p.Glu1797Val