Canonical Allele Identifier: CA1363339298
Gene: LAMB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49125071G= , CM000665.2:g.49125071G= GRCh38
NC_000003.11:g.49162504G= , CM000665.1:g.49162504G= GRCh37
NC_000003.10:g.49137508G= NCBI36
NG_008094.1:g.13096C=
NG_054716.1:g.868C=

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.2819C= MANE Select ENSP00000307156.4:p.Ala940=
ENST00000305544.8:c.2819C= ENSP00000307156.4:p.Ala940=
ENST00000418109.5:c.2819C= ENSP00000388325.1:p.Ala940=
ENST00000462930.5:n.226C=
ENST00000464891.5:n.552C=
ENST00000483057.1:n.419C=
ENST00000486298.5:n.524C=
ENST00000542580.1:n.134C=
NM_002292.3:c.2819C= NP_002283.3:p.Ala940=
XM_005265127.3:c.2819C= XP_005265184.1:p.Ala940=
XM_005265127.4:c.2819C= XP_005265184.1:p.Ala940=
NM_002292.4:c.2819C= MANE Select NP_002283.3:p.Ala940=