Canonical Allele Identifier: CA2625672083

Gene: LTBP2

Linked Data

• gnomAD v4: 14-74500879-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74500879G>T , CM000676.2:g.74500879G>T	GRCh38
NC_000014.8:g.74967582G>T , CM000676.1:g.74967582G>T	GRCh37
NC_000014.7:g.74037335G>T	NCBI36
NG_021486.1:g.116453C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.*5C>A MANE Select	ENSP00000261978.4:n.*5C>A
ENST00000261978.8:c.*5C>A	ENSP00000261978.4:n.*5C>A
ENST00000553939.5:c.*250C>A	ENSP00000452110.1:n.*250C>A
ENST00000554861.1:n.689C>A
ENST00000556690.5:c.*5C>A	ENSP00000451477.1:n.*5C>A
NM_000428.2:c.*5C>A	NP_000419.1:n.*5C>A
XM_011536765.1:c.*5C>A	XP_011535067.1:n.*5C>A
XM_011536766.1:c.*5C>A	XP_011535068.1:n.*5C>A
XM_011536767.1:c.*5C>A	XP_011535069.1:n.*5C>A
XM_011536765.2:c.*5C>A	XP_011535067.1:n.*5C>A
NM_000428.3:c.*5C>A MANE Select	NP_000419.1:n.*5C>A