Canonical Allele Identifier: CA352716290

Gene: LAMB2

Linked Data

• gnomAD v4: 3-49125061-G-C
• MyVariant Identifiers: chr3:g.49162494G>C (hg19) ; chr3:g.49125061G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125061G>C , CM000665.2:g.49125061G>C	GRCh38
NC_000003.11:g.49162494G>C , CM000665.1:g.49162494G>C	GRCh37
NC_000003.10:g.49137498G>C	NCBI36
NG_008094.1:g.13106C>G
NG_054716.1:g.878C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000305544.9:c.2829C>G MANE Select	ENSP00000307156.4:p.Cys943Trp
ENST00000305544.8:c.2829C>G	ENSP00000307156.4:p.Cys943Trp
ENST00000418109.5:c.2829C>G	ENSP00000388325.1:p.Cys943Trp
ENST00000462930.5:n.236C>G
ENST00000464891.5:n.562C>G
ENST00000483057.1:n.429C>G
ENST00000486298.5:n.534C>G
ENST00000542580.1:n.144C>G
NM_002292.3:c.2829C>G	NP_002283.3:p.Cys943Trp
XM_005265127.3:c.2829C>G	XP_005265184.1:p.Cys943Trp
XM_005265127.4:c.2829C>G	XP_005265184.1:p.Cys943Trp
NM_002292.4:c.2829C>G MANE Select	NP_002283.3:p.Cys943Trp