Canonical Allele Identifier: CA2147075154

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503252G= , CM000676.2:g.74503252G=	GRCh38
NC_000014.8:g.74969955G= , CM000676.1:g.74969955G=	GRCh37
NC_000014.7:g.74039708G=	NCBI36
NG_021486.1:g.114080C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000428.3:c.4855C= MANE Select	NP_000419.1:p.Gln1619=
ENST00000261978.9:c.4855C= MANE Select	ENSP00000261978.4:p.Gln1619=
NM_000428.2:c.4855C=	NP_000419.1:p.Gln1619=
ENST00000261978.8:c.4855C=	ENSP00000261978.4:p.Gln1619=
ENST00000553939.5:c.4855C=	ENSP00000452110.1:p.Gln1619=
ENST00000556690.5:c.4723C=	ENSP00000451477.1:p.Gln1575=
XM_011536765.1:c.4474C=	XP_011535067.1:p.Gln1492=
XM_011536765.2:c.4474C=	XP_011535067.1:p.Gln1492=
XM_011536766.1:c.4396C=	XP_011535068.1:p.Gln1466=
XM_011536767.1:c.4372C=	XP_011535069.1:p.Gln1458=