Canonical Allele Identifier: CA1363339339

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125102G= , CM000665.2:g.49125102G=	GRCh38
NC_000003.11:g.49162535G= , CM000665.1:g.49162535G=	GRCh37
NC_000003.10:g.49137539G=	NCBI36
NG_008094.1:g.13065C=
NG_054716.1:g.837C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2788C= MANE Select	ENSP00000307156.4:p.Pro930=
ENST00000305544.8:c.2788C=	ENSP00000307156.4:p.Pro930=
ENST00000418109.5:c.2788C=	ENSP00000388325.1:p.Pro930=
ENST00000462930.5:n.195C=
ENST00000464891.5:n.521C=
ENST00000483057.1:n.388C=
ENST00000486298.5:n.493C=
ENST00000542580.1:n.103C=
NM_002292.3:c.2788C=	NP_002283.3:p.Pro930=
XM_005265127.3:c.2788C=	XP_005265184.1:p.Pro930=
XM_005265127.4:c.2788C=	XP_005265184.1:p.Pro930=
NM_002292.4:c.2788C= MANE Select	NP_002283.3:p.Pro930=