Canonical Allele Identifier: CA1363339546
Gene: LAMB2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49125248C= , CM000665.2:g.49125248C= GRCh38
NC_000003.11:g.49162681C= , CM000665.1:g.49162681C= GRCh37
NC_000003.10:g.49137685C= NCBI36
NG_008094.1:g.12919G=
NG_054716.1:g.691G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.2720+5G= MANE Select ENSP00000307156.4:n.2720+5G=
ENST00000305544.8:c.2720+5G= ENSP00000307156.4:n.2720+5G=
ENST00000418109.5:c.2720+5G= ENSP00000388325.1:n.2720+5G=
ENST00000462930.5:n.127+5G=
ENST00000464891.5:n.453+21G=
ENST00000483057.1:n.320+5G=
ENST00000486298.5:n.426-79G=
NM_002292.3:c.2720+5G= NP_002283.3:n.2720+5G=
XM_005265127.3:c.2720+5G= XP_005265184.1:n.2720+5G=
XM_005265127.4:c.2720+5G= XP_005265184.1:n.2720+5G=
NM_002292.4:c.2720+5G= MANE Select NP_002283.3:n.2720+5G=
Search 100 bp 5'
Search 100 bp 3'