Canonical Allele Identifier: CA352715598

Gene: LAMB2

Linked Data

• gnomAD v4: 3-49125014-C-T
• MyVariant Identifiers: chr3:g.49162447C>T (hg19) ; chr3:g.49125014C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125014C>T , CM000665.2:g.49125014C>T	GRCh38
NC_000003.11:g.49162447C>T , CM000665.1:g.49162447C>T	GRCh37
NC_000003.10:g.49137451C>T	NCBI36
NG_008094.1:g.13153G>A
NG_054716.1:g.925G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2876G>A MANE Select	ENSP00000307156.4:p.Gly959Asp
ENST00000305544.8:c.2876G>A	ENSP00000307156.4:p.Gly959Asp
ENST00000418109.5:c.2876G>A	ENSP00000388325.1:p.Gly959Asp
ENST00000462930.5:n.283G>A
ENST00000464891.5:n.609G>A
ENST00000483057.1:n.476G>A
ENST00000486298.5:n.581G>A
ENST00000542580.1:n.191G>A
NM_002292.3:c.2876G>A	NP_002283.3:p.Gly959Asp
XM_005265127.3:c.2876G>A	XP_005265184.1:p.Gly959Asp
XM_005265127.4:c.2876G>A	XP_005265184.1:p.Gly959Asp
NM_002292.4:c.2876G>A MANE Select	NP_002283.3:p.Gly959Asp