Canonical Allele Identifier: CA433834122

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162509G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125076G>A , CM000665.2:g.49125076G>A	GRCh38
NC_000003.11:g.49162509G>A , CM000665.1:g.49162509G>A	GRCh37
NC_000003.10:g.49137513G>A	NCBI36
NG_008094.1:g.13091C>T
NG_054716.1:g.863C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2814C>T MANE Select	ENSP00000307156.4:p.His938=
ENST00000305544.8:c.2814C>T	ENSP00000307156.4:p.His938=
ENST00000418109.5:c.2814C>T	ENSP00000388325.1:p.His938=
ENST00000462930.5:n.221C>T
ENST00000464891.5:n.547C>T
ENST00000483057.1:n.414C>T
ENST00000486298.5:n.519C>T
ENST00000542580.1:n.129C>T
NM_002292.3:c.2814C>T	NP_002283.3:p.His938=
XM_005265127.3:c.2814C>T	XP_005265184.1:p.His938=
XM_005265127.4:c.2814C>T	XP_005265184.1:p.His938=
NM_002292.4:c.2814C>T MANE Select	NP_002283.3:p.His938=