Canonical Allele Identifier: CA352720895

Gene: LAMB2

Linked Data

• dbSNP Id: rs1412080788
• gnomAD v3: 3-49125470-G-A
• gnomAD v4: 3-49125470-G-A
• MyVariant Identifiers: chr3:g.49162903G>A (hg19) ; chr3:g.49125470G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125470G>A , CM000665.2:g.49125470G>A	GRCh38
NC_000003.11:g.49162903G>A , CM000665.1:g.49162903G>A	GRCh37
NC_000003.10:g.49137907G>A	NCBI36
NG_008094.1:g.12697C>T
NG_054716.1:g.469C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2503C>T MANE Select	ENSP00000307156.4:p.His835Tyr
ENST00000305544.8:c.2503C>T	ENSP00000307156.4:p.His835Tyr
ENST00000418109.5:c.2503C>T	ENSP00000388325.1:p.His835Tyr
ENST00000464891.5:n.252C>T
ENST00000477701.1:n.376C>T
ENST00000483057.1:n.103C>T
ENST00000486298.5:n.426-301C>T
NM_002292.3:c.2503C>T	NP_002283.3:p.His835Tyr
XM_005265127.3:c.2503C>T	XP_005265184.1:p.His835Tyr
XM_005265127.4:c.2503C>T	XP_005265184.1:p.His835Tyr
NM_002292.4:c.2503C>T MANE Select	NP_002283.3:p.His835Tyr