Canonical Allele Identifier: CA2665695271

Gene: LAMB2

Linked Data

• gnomAD v4: 3-49122850-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122851del , CM000665.2:g.49122851del	GRCh38
NC_000003.11:g.49160284del , CM000665.1:g.49160284del	GRCh37
NC_000003.10:g.49135288del	NCBI36
NG_008094.1:g.15316del
NG_054716.1:g.3088del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4426del MANE Select	ENSP00000307156.4:p.Arg1476GlufsTer?
ENST00000305544.8:c.4426del	ENSP00000307156.4:p.Arg1476GlufsTer?
ENST00000418109.5:c.4426del	ENSP00000388325.1:p.Arg1476GlufsTer?
ENST00000469665.1:n.735del
NM_002292.3:c.4426del	NP_002283.3:p.Arg1476GlufsTer?
XM_005265127.3:c.4426del	XP_005265184.1:p.Arg1476GlufsTer?
XM_005265127.4:c.4426del	XP_005265184.1:p.Arg1476GlufsTer?
NM_002292.4:c.4426del MANE Select	NP_002283.3:p.Arg1476GlufsTer?