Canonical Allele Identifier: CA352720826

Gene: LAMB2

Linked Data

• ClinVar Variation Id: 1062779
• ClinVar RCV Id: RCV001372535
• dbSNP Id: rs2107639681
• MyVariant Identifiers: chr3:g.49162897C>T (hg19) ; chr3:g.49125464C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125464C>T , CM000665.2:g.49125464C>T	GRCh38
NC_000003.11:g.49162897C>T , CM000665.1:g.49162897C>T	GRCh37
NC_000003.10:g.49137901C>T	NCBI36
NG_008094.1:g.12703G>A
NG_054716.1:g.475G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2509G>A MANE Select	ENSP00000307156.4:p.Gly837Arg
ENST00000305544.8:c.2509G>A	ENSP00000307156.4:p.Gly837Arg
ENST00000418109.5:c.2509G>A	ENSP00000388325.1:p.Gly837Arg
ENST00000464891.5:n.258G>A
ENST00000477701.1:n.382G>A
ENST00000483057.1:n.109G>A
ENST00000486298.5:n.426-295G>A
NM_002292.3:c.2509G>A	NP_002283.3:p.Gly837Arg
XM_005265127.3:c.2509G>A	XP_005265184.1:p.Gly837Arg
XM_005265127.4:c.2509G>A	XP_005265184.1:p.Gly837Arg
NM_002292.4:c.2509G>A MANE Select	NP_002283.3:p.Gly837Arg