Canonical Allele Identifier: CA1363339726

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125457A= , CM000665.2:g.49125457A=	GRCh38
NC_000003.11:g.49162890A= , CM000665.1:g.49162890A=	GRCh37
NC_000003.10:g.49137894A=	NCBI36
NG_008094.1:g.12710T=
NG_054716.1:g.482T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2516T= MANE Select	ENSP00000307156.4:p.Leu839=
ENST00000305544.8:c.2516T=	ENSP00000307156.4:p.Leu839=
ENST00000418109.5:c.2516T=	ENSP00000388325.1:p.Leu839=
ENST00000464891.5:n.265T=
ENST00000477701.1:n.389T=
ENST00000483057.1:n.116T=
ENST00000486298.5:n.426-288T=
NM_002292.3:c.2516T=	NP_002283.3:p.Leu839=
XM_005265127.3:c.2516T=	XP_005265184.1:p.Leu839=
XM_005265127.4:c.2516T=	XP_005265184.1:p.Leu839=
NM_002292.4:c.2516T= MANE Select	NP_002283.3:p.Leu839=