Canonical Allele Identifier: CA2665699818

Gene: LAMB2

Linked Data

• gnomAD v4: 3-49132086-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49132088dup , CM000665.2:g.49132088dup	GRCh38
NC_000003.11:g.49169521dup , CM000665.1:g.49169521dup	GRCh37
NC_000003.10:g.49144525dup	NCBI36
NG_008094.1:g.6080dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.459+29dup MANE Select	ENSP00000307156.4:n.459+29dup
ENST00000305544.8:c.459+29dup	ENSP00000307156.4:n.459+29dup
ENST00000418109.5:c.459+29dup	ENSP00000388325.1:n.459+29dup
ENST00000494831.1:c.12+29dup	ENSP00000444751.1:n.12+29dup
NM_002292.3:c.459+29dup	NP_002283.3:n.459+29dup
XM_005265127.3:c.459+29dup	XP_005265184.1:n.459+29dup
XM_005265127.4:c.459+29dup	XP_005265184.1:n.459+29dup
NM_002292.4:c.459+29dup MANE Select	NP_002283.3:n.459+29dup