Canonical Allele Identifier: CA487155752

Gene: LTBP2

Linked Data

• MyVariant Identifiers: chr14:g.74967659G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74500956G>C , CM000676.2:g.74500956G>C	GRCh38
NC_000014.8:g.74967659G>C , CM000676.1:g.74967659G>C	GRCh37
NC_000014.7:g.74037412G>C	NCBI36
NG_021486.1:g.116376C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.5394C>G MANE Select	ENSP00000261978.4:p.Gly1798=
ENST00000261978.8:c.5394C>G	ENSP00000261978.4:p.Gly1798=
ENST00000553939.5:c.*173C>G	ENSP00000452110.1:n.*173C>G
ENST00000554861.1:n.612C>G
ENST00000556690.5:c.5262C>G	ENSP00000451477.1:p.Gly1754=
NM_000428.2:c.5394C>G	NP_000419.1:p.Gly1798=
XM_011536765.1:c.5013C>G	XP_011535067.1:p.Gly1671=
XM_011536766.1:c.4935C>G	XP_011535068.1:p.Gly1645=
XM_011536767.1:c.4911C>G	XP_011535069.1:p.Gly1637=
XM_011536765.2:c.5013C>G	XP_011535067.1:p.Gly1671=
NM_000428.3:c.5394C>G MANE Select	NP_000419.1:p.Gly1798=