Canonical Allele Identifier: CA708512889

Gene: LTBP2

Linked Data

• dbSNP Id: rs1410785257
• MyVariant Identifiers: chr14:g.74967584C>T (hg19) ; chr14:g.74500881C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74500881C>T , CM000676.2:g.74500881C>T	GRCh38
NC_000014.8:g.74967584C>T , CM000676.1:g.74967584C>T	GRCh37
NC_000014.7:g.74037337C>T	NCBI36
NG_021486.1:g.116451G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.*3G>A MANE Select	ENSP00000261978.4:n.*3G>A
ENST00000261978.8:c.*3G>A	ENSP00000261978.4:n.*3G>A
ENST00000553939.5:c.*248G>A	ENSP00000452110.1:n.*248G>A
ENST00000554861.1:n.687G>A
ENST00000556690.5:c.*3G>A	ENSP00000451477.1:n.*3G>A
NM_000428.2:c.*3G>A	NP_000419.1:n.*3G>A
XM_011536765.1:c.*3G>A	XP_011535067.1:n.*3G>A
XM_011536766.1:c.*3G>A	XP_011535068.1:n.*3G>A
XM_011536767.1:c.*3G>A	XP_011535069.1:n.*3G>A
XM_011536765.2:c.*3G>A	XP_011535067.1:n.*3G>A
NM_000428.3:c.*3G>A MANE Select	NP_000419.1:n.*3G>A