Canonical Allele Identifier: CA2393821

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49123003C>G , CM000665.2:g.49123003C>G	GRCh38
NC_000003.11:g.49160436C>G , CM000665.1:g.49160436C>G	GRCh37
NC_000003.10:g.49135440C>G	NCBI36
NG_008094.1:g.15164G>C
NG_054716.1:g.2936G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002292.4:c.4274G>C MANE Select	NP_002283.3:p.Gly1425Ala
ENST00000305544.9:c.4274G>C MANE Select	ENSP00000307156.4:p.Gly1425Ala
NM_002292.3:c.4274G>C	NP_002283.3:p.Gly1425Ala
ENST00000305544.8:c.4274G>C	ENSP00000307156.4:p.Gly1425Ala
ENST00000418109.5:c.4274G>C	ENSP00000388325.1:p.Gly1425Ala
ENST00000469665.1:n.583G>C
XM_005265127.3:c.4274G>C	XP_005265184.1:p.Gly1425Ala
XM_005265127.4:c.4274G>C	XP_005265184.1:p.Gly1425Ala