Canonical Allele Identifier: CA1363339779

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122969G= , CM000665.2:g.49122969G=	GRCh38
NC_000003.11:g.49160402G= , CM000665.1:g.49160402G=	GRCh37
NC_000003.10:g.49135406G=	NCBI36
NG_008094.1:g.15198C=
NG_054716.1:g.2970C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4308C= MANE Select	ENSP00000307156.4:p.Arg1436=
ENST00000305544.8:c.4308C=	ENSP00000307156.4:p.Arg1436=
ENST00000418109.5:c.4308C=	ENSP00000388325.1:p.Arg1436=
ENST00000469665.1:n.617C=
NM_002292.3:c.4308C=	NP_002283.3:p.Arg1436=
XM_005265127.3:c.4308C=	XP_005265184.1:p.Arg1436=
XM_005265127.4:c.4308C=	XP_005265184.1:p.Arg1436=
NM_002292.4:c.4308C= MANE Select	NP_002283.3:p.Arg1436=