Canonical Allele Identifier: CA352716853
Gene: LAMB2 HGNC NCBI

Linked Data

dbSNP Id: rs776225413
gnomAD v4: 3-49125108-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49125108G>A , CM000665.2:g.49125108G>A GRCh38
NC_000003.11:g.49162541G>A , CM000665.1:g.49162541G>A GRCh37
NC_000003.10:g.49137545G>A NCBI36
NG_008094.1:g.13059C>T
NG_054716.1:g.831C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.2782C>T MANE Select ENSP00000307156.4:p.Pro928Ser
ENST00000305544.8:c.2782C>T ENSP00000307156.4:p.Pro928Ser
ENST00000418109.5:c.2782C>T ENSP00000388325.1:p.Pro928Ser
ENST00000462930.5:n.189C>T
ENST00000464891.5:n.515C>T
ENST00000483057.1:n.382C>T
ENST00000486298.5:n.487C>T
ENST00000542580.1:n.97C>T
NM_002292.3:c.2782C>T NP_002283.3:p.Pro928Ser
XM_005265127.3:c.2782C>T XP_005265184.1:p.Pro928Ser
XM_005265127.4:c.2782C>T XP_005265184.1:p.Pro928Ser
NM_002292.4:c.2782C>T MANE Select NP_002283.3:p.Pro928Ser