Canonical Allele Identifier: CA2563200873

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125491G>T , CM000665.2:g.49125491G>T	GRCh38
NC_000003.11:g.49162924G>T , CM000665.1:g.49162924G>T	GRCh37
NC_000003.10:g.49137928G>T	NCBI36
NG_008094.1:g.12676C>A
NG_054716.1:g.448C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2489-7C>A MANE Select	ENSP00000307156.4:n.2489-7C>A
ENST00000305544.8:c.2489-7C>A	ENSP00000307156.4:n.2489-7C>A
ENST00000418109.5:c.2489-7C>A	ENSP00000388325.1:n.2489-7C>A
ENST00000464891.5:n.231C>A
ENST00000477701.1:n.362-7C>A
ENST00000483057.1:n.82C>A
ENST00000486298.5:n.426-322C>A
NM_002292.3:c.2489-7C>A	NP_002283.3:n.2489-7C>A
XM_005265127.3:c.2489-7C>A	XP_005265184.1:n.2489-7C>A
XM_005265127.4:c.2489-7C>A	XP_005265184.1:n.2489-7C>A
NM_002292.4:c.2489-7C>A MANE Select	NP_002283.3:n.2489-7C>A