Canonical Allele Identifier: CA1363339728

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125458G= , CM000665.2:g.49125458G=	GRCh38
NC_000003.11:g.49162891G= , CM000665.1:g.49162891G=	GRCh37
NC_000003.10:g.49137895G=	NCBI36
NG_008094.1:g.12709C=
NG_054716.1:g.481C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2515C= MANE Select	ENSP00000307156.4:p.Leu839=
ENST00000305544.8:c.2515C=	ENSP00000307156.4:p.Leu839=
ENST00000418109.5:c.2515C=	ENSP00000388325.1:p.Leu839=
ENST00000464891.5:n.264C=
ENST00000477701.1:n.388C=
ENST00000483057.1:n.115C=
ENST00000486298.5:n.426-289C=
NM_002292.3:c.2515C=	NP_002283.3:p.Leu839=
XM_005265127.3:c.2515C=	XP_005265184.1:p.Leu839=
XM_005265127.4:c.2515C=	XP_005265184.1:p.Leu839=
NM_002292.4:c.2515C= MANE Select	NP_002283.3:p.Leu839=