Canonical Allele Identifier: CA1363339265
Gene: LAMB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49125011T= , CM000665.2:g.49125011T= GRCh38
NC_000003.11:g.49162444T= , CM000665.1:g.49162444T= GRCh37
NC_000003.10:g.49137448T= NCBI36
NG_008094.1:g.13156A=
NG_054716.1:g.928A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.2879A= MANE Select ENSP00000307156.4:p.Tyr960=
ENST00000305544.8:c.2879A= ENSP00000307156.4:p.Tyr960=
ENST00000418109.5:c.2879A= ENSP00000388325.1:p.Tyr960=
ENST00000462930.5:n.286A=
ENST00000464891.5:n.612A=
ENST00000483057.1:n.479A=
ENST00000486298.5:n.584A=
ENST00000542580.1:n.194A=
NM_002292.3:c.2879A= NP_002283.3:p.Tyr960=
XM_005265127.3:c.2879A= XP_005265184.1:p.Tyr960=
XM_005265127.4:c.2879A= XP_005265184.1:p.Tyr960=
NM_002292.4:c.2879A= MANE Select NP_002283.3:p.Tyr960=