Canonical Allele Identifier: CA2147122458

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74611621G= , CM000676.2:g.74611621G=	GRCh38
NC_000014.8:g.75078324G= , CM000676.1:g.75078324G=	GRCh37
NC_000014.7:g.74148077G=	NCBI36
NG_021486.1:g.5711C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.324C= MANE Select	ENSP00000261978.4:p.Arg108=
ENST00000261978.8:c.324C=	ENSP00000261978.4:p.Arg108=
ENST00000553939.5:c.324C=	ENSP00000452110.1:p.Arg108=
ENST00000556690.5:c.324C=	ENSP00000451477.1:p.Arg108=
ENST00000557425.1:n.123+425C=
NM_000428.2:c.324C=	NP_000419.1:p.Arg108=
XM_011536765.1:c.324C=	XP_011535067.1:p.Arg108=
XM_011536767.1:c.11+6963C=	XP_011535069.1:n.11+6963C=
XM_011536765.2:c.324C=	XP_011535067.1:p.Arg108=
NM_000428.3:c.324C= MANE Select	NP_000419.1:p.Arg108=