Canonical Allele Identifier: CA1363339627

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125333A= , CM000665.2:g.49125333A=	GRCh38
NC_000003.11:g.49162766A= , CM000665.1:g.49162766A=	GRCh37
NC_000003.10:g.49137770A=	NCBI36
NG_008094.1:g.12834T=
NG_054716.1:g.606T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2640T= MANE Select	ENSP00000307156.4:p.Asn880=
ENST00000305544.8:c.2640T=	ENSP00000307156.4:p.Asn880=
ENST00000418109.5:c.2640T=	ENSP00000388325.1:p.Asn880=
ENST00000462930.5:n.47T=
ENST00000464891.5:n.389T=
ENST00000477701.1:n.513T=
ENST00000483057.1:n.240T=
ENST00000486298.5:n.426-164T=
NM_002292.3:c.2640T=	NP_002283.3:p.Asn880=
XM_005265127.3:c.2640T=	XP_005265184.1:p.Asn880=
XM_005265127.4:c.2640T=	XP_005265184.1:p.Asn880=
NM_002292.4:c.2640T= MANE Select	NP_002283.3:p.Asn880=