Canonical Allele Identifier: CA352718563
Gene: LAMB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.49162750A>C (hg19) chr3:g.49125317A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49125317A>C , CM000665.2:g.49125317A>C GRCh38
NC_000003.11:g.49162750A>C , CM000665.1:g.49162750A>C GRCh37
NC_000003.10:g.49137754A>C NCBI36
NG_008094.1:g.12850T>G
NG_054716.1:g.622T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.2656T>G MANE Select ENSP00000307156.4:p.Cys886Gly
ENST00000305544.8:c.2656T>G ENSP00000307156.4:p.Cys886Gly
ENST00000418109.5:c.2656T>G ENSP00000388325.1:p.Cys886Gly
ENST00000462930.5:n.63T>G
ENST00000464891.5:n.405T>G
ENST00000477701.1:n.529T>G
ENST00000483057.1:n.256T>G
ENST00000486298.5:n.426-148T>G
NM_002292.3:c.2656T>G NP_002283.3:p.Cys886Gly
XM_005265127.3:c.2656T>G XP_005265184.1:p.Cys886Gly
XM_005265127.4:c.2656T>G XP_005265184.1:p.Cys886Gly
NM_002292.4:c.2656T>G MANE Select NP_002283.3:p.Cys886Gly
Search 100 bp 5'
Search 100 bp 3'