Canonical Allele Identifier: CA1363339214

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49124968A= , CM000665.2:g.49124968A=	GRCh38
NC_000003.11:g.49162401A= , CM000665.1:g.49162401A=	GRCh37
NC_000003.10:g.49137405A=	NCBI36
NG_008094.1:g.13199T=
NG_054716.1:g.971T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2884+38T= MANE Select	ENSP00000307156.4:n.2884+38T=
ENST00000305544.8:c.2884+38T=	ENSP00000307156.4:n.2884+38T=
ENST00000418109.5:c.2884+38T=	ENSP00000388325.1:n.2884+38T=
ENST00000462930.5:n.291+38T=
ENST00000464891.5:n.617+38T=
ENST00000483057.1:n.484+38T=
ENST00000542580.1:n.199+38T=
NM_002292.3:c.2884+38T=	NP_002283.3:n.2884+38T=
XM_005265127.3:c.2884+38T=	XP_005265184.1:n.2884+38T=
XM_005265127.4:c.2884+38T=	XP_005265184.1:n.2884+38T=
NM_002292.4:c.2884+38T= MANE Select	NP_002283.3:n.2884+38T=