Canonical Allele Identifier: CA1363339575

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122779C= , CM000665.2:g.49122779C=	GRCh38
NC_000003.11:g.49160212C= , CM000665.1:g.49160212C=	GRCh37
NC_000003.10:g.49135216C=	NCBI36
NG_008094.1:g.15388G=
NG_054716.1:g.3160G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4498G= MANE Select	ENSP00000307156.4:p.Ala1500=
ENST00000305544.8:c.4498G=	ENSP00000307156.4:p.Ala1500=
ENST00000418109.5:c.4498G=	ENSP00000388325.1:p.Ala1500=
ENST00000469665.1:n.807G=
NM_002292.3:c.4498G=	NP_002283.3:p.Ala1500=
XM_005265127.3:c.4498G=	XP_005265184.1:p.Ala1500=
XM_005265127.4:c.4498G=	XP_005265184.1:p.Ala1500=
NM_002292.4:c.4498G= MANE Select	NP_002283.3:p.Ala1500=