Canonical Allele Identifier: CA1363340163

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49123320G= , CM000665.2:g.49123320G=	GRCh38
NC_000003.11:g.49160753G= , CM000665.1:g.49160753G=	GRCh37
NC_000003.10:g.49135757G=	NCBI36
NG_008094.1:g.14847C=
NG_054716.1:g.2619C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4036C= MANE Select	ENSP00000307156.4:p.Arg1346=
ENST00000305544.8:c.4036C=	ENSP00000307156.4:p.Arg1346=
ENST00000418109.5:c.4036C=	ENSP00000388325.1:p.Arg1346=
ENST00000469665.1:n.266C=
NM_002292.3:c.4036C=	NP_002283.3:p.Arg1346=
XM_005265127.3:c.4036C=	XP_005265184.1:p.Arg1346=
XM_005265127.4:c.4036C=	XP_005265184.1:p.Arg1346=
NM_002292.4:c.4036C= MANE Select	NP_002283.3:p.Arg1346=