Canonical Allele Identifier: CA390384947

Gene: LTBP2

Linked Data

• MyVariant Identifiers: chr14:g.74970089T>C (hg19) ; chr14:g.74503386T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503386T>C , CM000676.2:g.74503386T>C	GRCh38
NC_000014.8:g.74970089T>C , CM000676.1:g.74970089T>C	GRCh37
NC_000014.7:g.74039842T>C	NCBI36
NG_021486.1:g.113946A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.4721A>G MANE Select	ENSP00000261978.4:p.Glu1574Gly
ENST00000261978.8:c.4721A>G	ENSP00000261978.4:p.Glu1574Gly
ENST00000553939.5:c.4721A>G	ENSP00000452110.1:p.Glu1574Gly
ENST00000556690.5:c.4589A>G	ENSP00000451477.1:p.Glu1530Gly
NM_000428.2:c.4721A>G	NP_000419.1:p.Glu1574Gly
XM_011536765.1:c.4340A>G	XP_011535067.1:p.Glu1447Gly
XM_011536766.1:c.4262A>G	XP_011535068.1:p.Glu1421Gly
XM_011536767.1:c.4238A>G	XP_011535069.1:p.Glu1413Gly
XM_011536765.2:c.4340A>G	XP_011535067.1:p.Glu1447Gly
NM_000428.3:c.4721A>G MANE Select	NP_000419.1:p.Glu1574Gly