Canonical Allele Identifier: CA2665695273
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49122850_49122851insG , CM000665.2:g.49122850_49122851insG GRCh38
NC_000003.11:g.49160283_49160284insG , CM000665.1:g.49160283_49160284insG GRCh37
NC_000003.10:g.49135287_49135288insG NCBI36
NG_008094.1:g.15316_15317insC
NG_054716.1:g.3088_3089insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.4426_4427insC MANE Select ENSP00000307156.4:p.Arg1476ThrfsTer4
ENST00000305544.8:c.4426_4427insC ENSP00000307156.4:p.Arg1476ThrfsTer4
ENST00000418109.5:c.4426_4427insC ENSP00000388325.1:p.Arg1476ThrfsTer4
ENST00000469665.1:n.735_736insC
NM_002292.3:c.4426_4427insC NP_002283.3:p.Arg1476ThrfsTer4
XM_005265127.3:c.4426_4427insC XP_005265184.1:p.Arg1476ThrfsTer4
XM_005265127.4:c.4426_4427insC XP_005265184.1:p.Arg1476ThrfsTer4
NM_002292.4:c.4426_4427insC MANE Select NP_002283.3:p.Arg1476ThrfsTer4