Canonical Allele Identifier: CA1363339533

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125233C= , CM000665.2:g.49125233C=	GRCh38
NC_000003.11:g.49162666C= , CM000665.1:g.49162666C=	GRCh37
NC_000003.10:g.49137670C=	NCBI36
NG_008094.1:g.12934G=
NG_054716.1:g.706G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2720+20G= MANE Select	ENSP00000307156.4:n.2720+20G=
ENST00000305544.8:c.2720+20G=	ENSP00000307156.4:n.2720+20G=
ENST00000418109.5:c.2720+20G=	ENSP00000388325.1:n.2720+20G=
ENST00000462930.5:n.127+20G=
ENST00000464891.5:n.453+36G=
ENST00000483057.1:n.320+20G=
ENST00000486298.5:n.426-64G=
NM_002292.3:c.2720+20G=	NP_002283.3:n.2720+20G=
XM_005265127.3:c.2720+20G=	XP_005265184.1:n.2720+20G=
XM_005265127.4:c.2720+20G=	XP_005265184.1:n.2720+20G=
NM_002292.4:c.2720+20G= MANE Select	NP_002283.3:n.2720+20G=