Canonical Allele Identifier: CA352718097
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49125280T>C , CM000665.2:g.49125280T>C GRCh38
NC_000003.11:g.49162713T>C , CM000665.1:g.49162713T>C GRCh37
NC_000003.10:g.49137717T>C NCBI36
NG_008094.1:g.12887A>G
NG_054716.1:g.659A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.2693A>G MANE Select ENSP00000307156.4:p.Asp898Gly
ENST00000305544.8:c.2693A>G ENSP00000307156.4:p.Asp898Gly
ENST00000418109.5:c.2693A>G ENSP00000388325.1:p.Asp898Gly
ENST00000462930.5:n.100A>G
ENST00000464891.5:n.442A>G
ENST00000483057.1:n.293A>G
ENST00000486298.5:n.426-111A>G
NM_002292.3:c.2693A>G NP_002283.3:p.Asp898Gly
XM_005265127.3:c.2693A>G XP_005265184.1:p.Asp898Gly
XM_005265127.4:c.2693A>G XP_005265184.1:p.Asp898Gly
NM_002292.4:c.2693A>G MANE Select NP_002283.3:p.Asp898Gly