Canonical Allele Identifier: CA1363339589

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125294G= , CM000665.2:g.49125294G=	GRCh38
NC_000003.11:g.49162727G= , CM000665.1:g.49162727G=	GRCh37
NC_000003.10:g.49137731G=	NCBI36
NG_008094.1:g.12873C=
NG_054716.1:g.645C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2679C= MANE Select	ENSP00000307156.4:p.Cys893=
ENST00000305544.8:c.2679C=	ENSP00000307156.4:p.Cys893=
ENST00000418109.5:c.2679C=	ENSP00000388325.1:p.Cys893=
ENST00000462930.5:n.86C=
ENST00000464891.5:n.428C=
ENST00000477701.1:n.552C=
ENST00000483057.1:n.279C=
ENST00000486298.5:n.426-125C=
NM_002292.3:c.2679C=	NP_002283.3:p.Cys893=
XM_005265127.3:c.2679C=	XP_005265184.1:p.Cys893=
XM_005265127.4:c.2679C=	XP_005265184.1:p.Cys893=
NM_002292.4:c.2679C= MANE Select	NP_002283.3:p.Cys893=