Canonical Allele Identifier: CA2665695219

Gene: LAMB2

Linked Data

• gnomAD v4: 3-49122839-TCTCAGCCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122840_49122848del , CM000665.2:g.49122840_49122848del	GRCh38
NC_000003.11:g.49160273_49160281del , CM000665.1:g.49160273_49160281del	GRCh37
NC_000003.10:g.49135277_49135285del	NCBI36
NG_008094.1:g.15319_15327del
NG_054716.1:g.3091_3099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4429_4437del MANE Select	ENSP00000307156.4:p.Val1477_Glu1479del
ENST00000305544.8:c.4429_4437del	ENSP00000307156.4:p.Val1477_Glu1479del
ENST00000418109.5:c.4429_4437del	ENSP00000388325.1:p.Val1477_Glu1479del
ENST00000469665.1:n.738_746del
NM_002292.3:c.4429_4437del	NP_002283.3:p.Val1477_Glu1479del
XM_005265127.3:c.4429_4437del	XP_005265184.1:p.Val1477_Glu1479del
XM_005265127.4:c.4429_4437del	XP_005265184.1:p.Val1477_Glu1479del
NM_002292.4:c.4429_4437del MANE Select	NP_002283.3:p.Val1477_Glu1479del