Canonical Allele Identifier: CA2665697260
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49124994_49125020del , CM000665.2:g.49124994_49125020del GRCh38
NC_000003.11:g.49162427_49162453del , CM000665.1:g.49162427_49162453del GRCh37
NC_000003.10:g.49137431_49137457del NCBI36
NG_008094.1:g.13155_13181del
NG_054716.1:g.927_953del

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.2878_2884+20del
ENST00000305544.8:c.2878_2884+20del
ENST00000418109.5:c.2878_2884+20del
ENST00000462930.5:n.285_291+20del
ENST00000464891.5:n.611_617+20del
ENST00000483057.1:n.478_484+20del
ENST00000542580.1:n.193_199+20del
NM_002292.3:c.2878_2884+20del
XM_005265127.3:c.2878_2884+20del
XM_005265127.4:c.2878_2884+20del
NM_002292.4:c.2878_2884+20del