Canonical Allele Identifier: CA352718764
Gene: LAMB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.49162762G>C (hg19) chr3:g.49125329G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49125329G>C , CM000665.2:g.49125329G>C GRCh38
NC_000003.11:g.49162762G>C , CM000665.1:g.49162762G>C GRCh37
NC_000003.10:g.49137766G>C NCBI36
NG_008094.1:g.12838C>G
NG_054716.1:g.610C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.2644C>G MANE Select ENSP00000307156.4:p.His882Asp
ENST00000305544.8:c.2644C>G ENSP00000307156.4:p.His882Asp
ENST00000418109.5:c.2644C>G ENSP00000388325.1:p.His882Asp
ENST00000462930.5:n.51C>G
ENST00000464891.5:n.393C>G
ENST00000477701.1:n.517C>G
ENST00000483057.1:n.244C>G
ENST00000486298.5:n.426-160C>G
NM_002292.3:c.2644C>G NP_002283.3:p.His882Asp
XM_005265127.3:c.2644C>G XP_005265184.1:p.His882Asp
XM_005265127.4:c.2644C>G XP_005265184.1:p.His882Asp
NM_002292.4:c.2644C>G MANE Select NP_002283.3:p.His882Asp
Search 100 bp 5'
Search 100 bp 3'