Canonical Allele Identifier: CA433833925

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162446G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125013G>A , CM000665.2:g.49125013G>A	GRCh38
NC_000003.11:g.49162446G>A , CM000665.1:g.49162446G>A	GRCh37
NC_000003.10:g.49137450G>A	NCBI36
NG_008094.1:g.13154C>T
NG_054716.1:g.926C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2877C>T MANE Select	ENSP00000307156.4:p.Gly959=
ENST00000305544.8:c.2877C>T	ENSP00000307156.4:p.Gly959=
ENST00000418109.5:c.2877C>T	ENSP00000388325.1:p.Gly959=
ENST00000462930.5:n.284C>T
ENST00000464891.5:n.610C>T
ENST00000483057.1:n.477C>T
ENST00000486298.5:n.582C>T
ENST00000542580.1:n.192C>T
NM_002292.3:c.2877C>T	NP_002283.3:p.Gly959=
XM_005265127.3:c.2877C>T	XP_005265184.1:p.Gly959=
XM_005265127.4:c.2877C>T	XP_005265184.1:p.Gly959=
NM_002292.4:c.2877C>T MANE Select	NP_002283.3:p.Gly959=