Canonical Allele Identifier: CA1363339287

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125050T= , CM000665.2:g.49125050T=	GRCh38
NC_000003.11:g.49162483T= , CM000665.1:g.49162483T=	GRCh37
NC_000003.10:g.49137487T=	NCBI36
NG_008094.1:g.13117A=
NG_054716.1:g.889A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2840A= MANE Select	ENSP00000307156.4:p.Glu947=
ENST00000305544.8:c.2840A=	ENSP00000307156.4:p.Glu947=
ENST00000418109.5:c.2840A=	ENSP00000388325.1:p.Glu947=
ENST00000462930.5:n.247A=
ENST00000464891.5:n.573A=
ENST00000483057.1:n.440A=
ENST00000486298.5:n.545A=
ENST00000542580.1:n.155A=
NM_002292.3:c.2840A=	NP_002283.3:p.Glu947=
XM_005265127.3:c.2840A=	XP_005265184.1:p.Glu947=
XM_005265127.4:c.2840A=	XP_005265184.1:p.Glu947=
NM_002292.4:c.2840A= MANE Select	NP_002283.3:p.Glu947=