Canonical Allele Identifier: CA1363339591
Gene: LAMB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49122794G= , CM000665.2:g.49122794G= GRCh38
NC_000003.11:g.49160227G= , CM000665.1:g.49160227G= GRCh37
NC_000003.10:g.49135231G= NCBI36
NG_008094.1:g.15373C=
NG_054716.1:g.3145C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.4483C= MANE Select ENSP00000307156.4:p.Leu1495=
ENST00000305544.8:c.4483C= ENSP00000307156.4:p.Leu1495=
ENST00000418109.5:c.4483C= ENSP00000388325.1:p.Leu1495=
ENST00000469665.1:n.792C=
NM_002292.3:c.4483C= NP_002283.3:p.Leu1495=
XM_005265127.3:c.4483C= XP_005265184.1:p.Leu1495=
XM_005265127.4:c.4483C= XP_005265184.1:p.Leu1495=
NM_002292.4:c.4483C= MANE Select NP_002283.3:p.Leu1495=