Canonical Allele Identifier: CA1363339714

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125442T= , CM000665.2:g.49125442T=	GRCh38
NC_000003.11:g.49162875T= , CM000665.1:g.49162875T=	GRCh37
NC_000003.10:g.49137879T=	NCBI36
NG_008094.1:g.12725A=
NG_054716.1:g.497A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2531A= MANE Select	ENSP00000307156.4:p.Glu844=
ENST00000305544.8:c.2531A=	ENSP00000307156.4:p.Glu844=
ENST00000418109.5:c.2531A=	ENSP00000388325.1:p.Glu844=
ENST00000464891.5:n.280A=
ENST00000477701.1:n.404A=
ENST00000483057.1:n.131A=
ENST00000486298.5:n.426-273A=
NM_002292.3:c.2531A=	NP_002283.3:p.Glu844=
XM_005265127.3:c.2531A=	XP_005265184.1:p.Glu844=
XM_005265127.4:c.2531A=	XP_005265184.1:p.Glu844=
NM_002292.4:c.2531A= MANE Select	NP_002283.3:p.Glu844=