Canonical Allele Identifier: CA1363342483

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49130334A= , CM000665.2:g.49130334A=	GRCh38
NC_000003.11:g.49167767A= , CM000665.1:g.49167767A=	GRCh37
NC_000003.10:g.49142771A=	NCBI36
NG_008094.1:g.7833T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305544.9:c.1122T= MANE Select	ENSP00000307156.4:p.Cys374=
ENST00000305544.8:c.1122T=	ENSP00000307156.4:p.Cys374=
ENST00000418109.5:c.1122T=	ENSP00000388325.1:p.Cys374=
NM_002292.3:c.1122T=	NP_002283.3:p.Cys374=
XM_005265127.3:c.1122T=	XP_005265184.1:p.Cys374=
XM_005265127.4:c.1122T=	XP_005265184.1:p.Cys374=
NM_002292.4:c.1122T= MANE Select	NP_002283.3:p.Cys374=