Canonical Allele Identifier: CA1363339324

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125094_49125095delinsGC , CM000665.2:g.49125094_49125095delinsGC	GRCh38
NC_000003.11:g.49162527_49162528delinsGC , CM000665.1:g.49162527_49162528delinsGC	GRCh37
NC_000003.10:g.49137531_49137532delinsGC	NCBI36
NG_008094.1:g.13072_13073delinsGC
NG_054716.1:g.844_845delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2795_2796delinsGC MANE Select	ENSP00000307156.4:p.Gly932=
ENST00000305544.8:c.2795_2796delinsGC	ENSP00000307156.4:p.Gly932=
ENST00000418109.5:c.2795_2796delinsGC	ENSP00000388325.1:p.Gly932=
ENST00000462930.5:n.202_203delinsGC
ENST00000464891.5:n.528_529delinsGC
ENST00000483057.1:n.395_396delinsGC
ENST00000486298.5:n.500_501delinsGC
ENST00000542580.1:n.110_111delinsGC
NM_002292.3:c.2795_2796delinsGC	NP_002283.3:p.Gly932=
XM_005265127.3:c.2795_2796delinsGC	XP_005265184.1:p.Gly932=
XM_005265127.4:c.2795_2796delinsGC	XP_005265184.1:p.Gly932=
NM_002292.4:c.2795_2796delinsGC MANE Select	NP_002283.3:p.Gly932=