Canonical Allele Identifier: CA1363339613

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125315G= , CM000665.2:g.49125315G=	GRCh38
NC_000003.11:g.49162748G= , CM000665.1:g.49162748G=	GRCh37
NC_000003.10:g.49137752G=	NCBI36
NG_008094.1:g.12852C=
NG_054716.1:g.624C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2658C= MANE Select	ENSP00000307156.4:p.Cys886=
ENST00000305544.8:c.2658C=	ENSP00000307156.4:p.Cys886=
ENST00000418109.5:c.2658C=	ENSP00000388325.1:p.Cys886=
ENST00000462930.5:n.65C=
ENST00000464891.5:n.407C=
ENST00000477701.1:n.531C=
ENST00000483057.1:n.258C=
ENST00000486298.5:n.426-146C=
NM_002292.3:c.2658C=	NP_002283.3:p.Cys886=
XM_005265127.3:c.2658C=	XP_005265184.1:p.Cys886=
XM_005265127.4:c.2658C=	XP_005265184.1:p.Cys886=
NM_002292.4:c.2658C= MANE Select	NP_002283.3:p.Cys886=