Canonical Allele Identifier: CA352717107
Gene: LAMB2 HGNC NCBI

Linked Data

dbSNP Id: rs1254687643
gnomAD v2: 3-49162562-C-T
gnomAD v3: 3-49125129-C-T
gnomAD v4: 3-49125129-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49125129C>T , CM000665.2:g.49125129C>T GRCh38
NC_000003.11:g.49162562C>T , CM000665.1:g.49162562C>T GRCh37
NC_000003.10:g.49137566C>T NCBI36
NG_008094.1:g.13038G>A
NG_054716.1:g.810G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.2761G>A MANE Select ENSP00000307156.4:p.Gly921Arg
ENST00000305544.8:c.2761G>A ENSP00000307156.4:p.Gly921Arg
ENST00000418109.5:c.2761G>A ENSP00000388325.1:p.Gly921Arg
ENST00000462930.5:n.168G>A
ENST00000464891.5:n.494G>A
ENST00000483057.1:n.361G>A
ENST00000486298.5:n.466G>A
ENST00000542580.1:n.76G>A
NM_002292.3:c.2761G>A NP_002283.3:p.Gly921Arg
XM_005265127.3:c.2761G>A XP_005265184.1:p.Gly921Arg
XM_005265127.4:c.2761G>A XP_005265184.1:p.Gly921Arg
NM_002292.4:c.2761G>A MANE Select NP_002283.3:p.Gly921Arg