Canonical Allele Identifier: CA1363339378

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125131T= , CM000665.2:g.49125131T=	GRCh38
NC_000003.11:g.49162564T= , CM000665.1:g.49162564T=	GRCh37
NC_000003.10:g.49137568T=	NCBI36
NG_008094.1:g.13036A=
NG_054716.1:g.808A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2759A= MANE Select	ENSP00000307156.4:p.Tyr920=
ENST00000305544.8:c.2759A=	ENSP00000307156.4:p.Tyr920=
ENST00000418109.5:c.2759A=	ENSP00000388325.1:p.Tyr920=
ENST00000462930.5:n.166A=
ENST00000464891.5:n.492A=
ENST00000483057.1:n.359A=
ENST00000486298.5:n.464A=
ENST00000542580.1:n.74A=
NM_002292.3:c.2759A=	NP_002283.3:p.Tyr920=
XM_005265127.3:c.2759A=	XP_005265184.1:p.Tyr920=
XM_005265127.4:c.2759A=	XP_005265184.1:p.Tyr920=
NM_002292.4:c.2759A= MANE Select	NP_002283.3:p.Tyr920=