Canonical Allele Identifier: CA2625668676

Gene: LTBP2

Linked Data

• gnomAD v4: 14-74503402-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503402A>G , CM000676.2:g.74503402A>G	GRCh38
NC_000014.8:g.74970105A>G , CM000676.1:g.74970105A>G	GRCh37
NC_000014.7:g.74039858A>G	NCBI36
NG_021486.1:g.113930T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261978.9:c.4721-16T>C MANE Select	ENSP00000261978.4:n.4721-16T>C
ENST00000261978.8:c.4721-16T>C	ENSP00000261978.4:n.4721-16T>C
ENST00000553939.5:c.4721-16T>C	ENSP00000452110.1:n.4721-16T>C
ENST00000556690.5:c.4589-16T>C	ENSP00000451477.1:n.4589-16T>C
NM_000428.2:c.4721-16T>C	NP_000419.1:n.4721-16T>C
XM_011536765.1:c.4340-16T>C	XP_011535067.1:n.4340-16T>C
XM_011536766.1:c.4262-16T>C	XP_011535068.1:n.4262-16T>C
XM_011536767.1:c.4238-16T>C	XP_011535069.1:n.4238-16T>C
XM_011536765.2:c.4340-16T>C	XP_011535067.1:n.4340-16T>C
NM_000428.3:c.4721-16T>C MANE Select	NP_000419.1:n.4721-16T>C