Canonical Allele Identifier: CA1363339274

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125021G= , CM000665.2:g.49125021G=	GRCh38
NC_000003.11:g.49162454G= , CM000665.1:g.49162454G=	GRCh37
NC_000003.10:g.49137458G=	NCBI36
NG_008094.1:g.13146C=
NG_054716.1:g.918C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2869C= MANE Select	ENSP00000307156.4:p.Arg957=
ENST00000305544.8:c.2869C=	ENSP00000307156.4:p.Arg957=
ENST00000418109.5:c.2869C=	ENSP00000388325.1:p.Arg957=
ENST00000462930.5:n.276C=
ENST00000464891.5:n.602C=
ENST00000483057.1:n.469C=
ENST00000486298.5:n.574C=
ENST00000542580.1:n.184C=
NM_002292.3:c.2869C=	NP_002283.3:p.Arg957=
XM_005265127.3:c.2869C=	XP_005265184.1:p.Arg957=
XM_005265127.4:c.2869C=	XP_005265184.1:p.Arg957=
NM_002292.4:c.2869C= MANE Select	NP_002283.3:p.Arg957=