Canonical Allele Identifier: CA1047736169

Gene: LAMB2

Linked Data

• gnomAD v3: 3-49125172-G-T
• gnomAD v4: 3-49125172-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125172G>T , CM000665.2:g.49125172G>T	GRCh38
NC_000003.11:g.49162605G>T , CM000665.1:g.49162605G>T	GRCh37
NC_000003.10:g.49137609G>T	NCBI36
NG_008094.1:g.12995C>A
NG_054716.1:g.767C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2721-3C>A MANE Select	ENSP00000307156.4:n.2721-3C>A
ENST00000305544.8:c.2721-3C>A	ENSP00000307156.4:n.2721-3C>A
ENST00000418109.5:c.2721-3C>A	ENSP00000388325.1:n.2721-3C>A
ENST00000462930.5:n.128-3C>A
ENST00000464891.5:n.454-3C>A
ENST00000483057.1:n.321-3C>A
ENST00000486298.5:n.426-3C>A
ENST00000542580.1:n.33C>A
NM_002292.3:c.2721-3C>A	NP_002283.3:n.2721-3C>A
XM_005265127.3:c.2721-3C>A	XP_005265184.1:n.2721-3C>A
XM_005265127.4:c.2721-3C>A	XP_005265184.1:n.2721-3C>A
NM_002292.4:c.2721-3C>A MANE Select	NP_002283.3:n.2721-3C>A