Canonical Allele Identifier: CA1363339632

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122840C= , CM000665.2:g.49122840C=	GRCh38
NC_000003.11:g.49160273C= , CM000665.1:g.49160273C=	GRCh37
NC_000003.10:g.49135277C=	NCBI36
NG_008094.1:g.15327G=
NG_054716.1:g.3099G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4437G= MANE Select	ENSP00000307156.4:p.Glu1479=
ENST00000305544.8:c.4437G=	ENSP00000307156.4:p.Glu1479=
ENST00000418109.5:c.4437G=	ENSP00000388325.1:p.Glu1479=
ENST00000469665.1:n.746G=
NM_002292.3:c.4437G=	NP_002283.3:p.Glu1479=
XM_005265127.3:c.4437G=	XP_005265184.1:p.Glu1479=
XM_005265127.4:c.4437G=	XP_005265184.1:p.Glu1479=
NM_002292.4:c.4437G= MANE Select	NP_002283.3:p.Glu1479=