Canonical Allele Identifier: CA7269575
Community Standard Title: NM_000428.3(LTBP2):c.2326G>A (p.Val776Ile)
Gene: LTBP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74528525C>T , CM000676.2:g.74528525C>T GRCh38
NC_000014.8:g.74995228C>T , CM000676.1:g.74995228C>T GRCh37
NC_000014.7:g.74064981C>T NCBI36
NG_021486.1:g.88807G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000428.3:c.2326G>A MANE Select NP_000419.1:p.Val776Ile
ENST00000261978.9:c.2326G>A MANE Select ENSP00000261978.4:p.Val776Ile
NM_000428.2:c.2326G>A NP_000419.1:p.Val776Ile
ENST00000261978.8:c.2326G>A ENSP00000261978.4:p.Val776Ile
ENST00000553939.5:c.2326G>A ENSP00000452110.1:p.Val776Ile
ENST00000556690.5:c.2326G>A ENSP00000451477.1:p.Val776Ile
XM_011536765.1:c.1988-1159G>A XP_011535067.1:n.1988-1159G>A
XM_011536765.2:c.1988-1159G>A XP_011535067.1:n.1988-1159G>A
XM_011536766.1:c.1867G>A XP_011535068.1:p.Val623Ile
XM_011536767.1:c.1843G>A XP_011535069.1:p.Val615Ile