Canonical Allele Identifier: CA1363339593

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122795G= , CM000665.2:g.49122795G=	GRCh38
NC_000003.11:g.49160228G= , CM000665.1:g.49160228G=	GRCh37
NC_000003.10:g.49135232G=	NCBI36
NG_008094.1:g.15372C=
NG_054716.1:g.3144C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4482C= MANE Select	ENSP00000307156.4:p.Ala1494=
ENST00000305544.8:c.4482C=	ENSP00000307156.4:p.Ala1494=
ENST00000418109.5:c.4482C=	ENSP00000388325.1:p.Ala1494=
ENST00000469665.1:n.791C=
NM_002292.3:c.4482C=	NP_002283.3:p.Ala1494=
XM_005265127.3:c.4482C=	XP_005265184.1:p.Ala1494=
XM_005265127.4:c.4482C=	XP_005265184.1:p.Ala1494=
NM_002292.4:c.4482C= MANE Select	NP_002283.3:p.Ala1494=