Canonical Allele Identifier: CA1363339260

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125008G= , CM000665.2:g.49125008G=	GRCh38
NC_000003.11:g.49162441G= , CM000665.1:g.49162441G=	GRCh37
NC_000003.10:g.49137445G=	NCBI36
NG_008094.1:g.13159C=
NG_054716.1:g.931C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2882C= MANE Select	ENSP00000307156.4:p.Thr961=
ENST00000305544.8:c.2882C=	ENSP00000307156.4:p.Thr961=
ENST00000418109.5:c.2882C=	ENSP00000388325.1:p.Thr961=
ENST00000462930.5:n.289C=
ENST00000464891.5:n.615C=
ENST00000483057.1:n.482C=
ENST00000486298.5:n.587C=
ENST00000542580.1:n.197C=
NM_002292.3:c.2882C=	NP_002283.3:p.Thr961=
XM_005265127.3:c.2882C=	XP_005265184.1:p.Thr961=
XM_005265127.4:c.2882C=	XP_005265184.1:p.Thr961=
NM_002292.4:c.2882C= MANE Select	NP_002283.3:p.Thr961=