Canonical Allele Identifier: CA2147075386

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503476G= , CM000676.2:g.74503476G=	GRCh38
NC_000014.8:g.74970179G= , CM000676.1:g.74970179G=	GRCh37
NC_000014.7:g.74039932G=	NCBI36
NG_021486.1:g.113856C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.4713C= MANE Select	ENSP00000261978.4:p.Ser1571=
ENST00000261978.8:c.4713C=	ENSP00000261978.4:p.Ser1571=
ENST00000553939.5:c.4713C=	ENSP00000452110.1:p.Ser1571=
ENST00000556690.5:c.4581C=	ENSP00000451477.1:p.Ser1527=
NM_000428.2:c.4713C=	NP_000419.1:p.Ser1571=
XM_011536765.1:c.4332C=	XP_011535067.1:p.Ser1444=
XM_011536766.1:c.4254C=	XP_011535068.1:p.Ser1418=
XM_011536767.1:c.4230C=	XP_011535069.1:p.Ser1410=
XM_011536765.2:c.4332C=	XP_011535067.1:p.Ser1444=
NM_000428.3:c.4713C= MANE Select	NP_000419.1:p.Ser1571=