Canonical Allele Identifier: CA487155781

Gene: LTBP2

Linked Data

• gnomAD v4: 14-74501001-C-A
• MyVariant Identifiers: chr14:g.74967704C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74501001C>A , CM000676.2:g.74501001C>A	GRCh38
NC_000014.8:g.74967704C>A , CM000676.1:g.74967704C>A	GRCh37
NC_000014.7:g.74037457C>A	NCBI36
NG_021486.1:g.116331G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.5349G>T MANE Select	ENSP00000261978.4:p.Gly1783=
ENST00000261978.8:c.5349G>T	ENSP00000261978.4:p.Gly1783=
ENST00000553939.5:c.*128G>T	ENSP00000452110.1:n.*128G>T
ENST00000554861.1:n.567G>T
ENST00000556690.5:c.5217G>T	ENSP00000451477.1:p.Gly1739=
NM_000428.2:c.5349G>T	NP_000419.1:p.Gly1783=
XM_011536765.1:c.4968G>T	XP_011535067.1:p.Gly1656=
XM_011536766.1:c.4890G>T	XP_011535068.1:p.Gly1630=
XM_011536767.1:c.4866G>T	XP_011535069.1:p.Gly1622=
XM_011536765.2:c.4968G>T	XP_011535067.1:p.Gly1656=
NM_000428.3:c.5349G>T MANE Select	NP_000419.1:p.Gly1783=