Canonical Allele Identifier: CA2147075321

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503413T= , CM000676.2:g.74503413T=	GRCh38
NC_000014.8:g.74970116T= , CM000676.1:g.74970116T=	GRCh37
NC_000014.7:g.74039869T=	NCBI36
NG_021486.1:g.113919A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.4721-27A= MANE Select	ENSP00000261978.4:n.4721-27A=
ENST00000261978.8:c.4721-27A=	ENSP00000261978.4:n.4721-27A=
ENST00000553939.5:c.4721-27A=	ENSP00000452110.1:n.4721-27A=
ENST00000556690.5:c.4589-27A=	ENSP00000451477.1:n.4589-27A=
NM_000428.2:c.4721-27A=	NP_000419.1:n.4721-27A=
XM_011536765.1:c.4340-27A=	XP_011535067.1:n.4340-27A=
XM_011536766.1:c.4262-27A=	XP_011535068.1:n.4262-27A=
XM_011536767.1:c.4238-27A=	XP_011535069.1:n.4238-27A=
XM_011536765.2:c.4340-27A=	XP_011535067.1:n.4340-27A=
NM_000428.3:c.4721-27A= MANE Select	NP_000419.1:n.4721-27A=