Canonical Allele Identifier: CA647881389

Gene: LAMB2

Linked Data

• COSMIC: COSN24386082

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49124993C>T , CM000665.2:g.49124993C>T	GRCh38
NC_000003.11:g.49162426C>T , CM000665.1:g.49162426C>T	GRCh37
NC_000003.10:g.49137430C>T	NCBI36
NG_008094.1:g.13174G>A
NG_054716.1:g.946G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2884+13G>A MANE Select	ENSP00000307156.4:n.2884+13G>A
ENST00000305544.8:c.2884+13G>A	ENSP00000307156.4:n.2884+13G>A
ENST00000418109.5:c.2884+13G>A	ENSP00000388325.1:n.2884+13G>A
ENST00000462930.5:n.291+13G>A
ENST00000464891.5:n.617+13G>A
ENST00000483057.1:n.484+13G>A
ENST00000542580.1:n.199+13G>A
NM_002292.3:c.2884+13G>A	NP_002283.3:n.2884+13G>A
XM_005265127.3:c.2884+13G>A	XP_005265184.1:n.2884+13G>A
XM_005265127.4:c.2884+13G>A	XP_005265184.1:n.2884+13G>A
NM_002292.4:c.2884+13G>A MANE Select	NP_002283.3:n.2884+13G>A