Canonical Allele Identifier: CA1363339300

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125073A= , CM000665.2:g.49125073A=	GRCh38
NC_000003.11:g.49162506A= , CM000665.1:g.49162506A=	GRCh37
NC_000003.10:g.49137510A=	NCBI36
NG_008094.1:g.13094T=
NG_054716.1:g.866T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2817T= MANE Select	ENSP00000307156.4:p.Phe939=
ENST00000305544.8:c.2817T=	ENSP00000307156.4:p.Phe939=
ENST00000418109.5:c.2817T=	ENSP00000388325.1:p.Phe939=
ENST00000462930.5:n.224T=
ENST00000464891.5:n.550T=
ENST00000483057.1:n.417T=
ENST00000486298.5:n.522T=
ENST00000542580.1:n.132T=
NM_002292.3:c.2817T=	NP_002283.3:p.Phe939=
XM_005265127.3:c.2817T=	XP_005265184.1:p.Phe939=
XM_005265127.4:c.2817T=	XP_005265184.1:p.Phe939=
NM_002292.4:c.2817T= MANE Select	NP_002283.3:p.Phe939=