Canonical Allele Identifier: CA74487868
Gene: LAMB2 HGNC NCBI

Linked Data

dbSNP Id: rs34313942

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49130742del , CM000665.2:g.49130742del GRCh38
NC_000003.11:g.49168175del , CM000665.1:g.49168175del GRCh37
NC_000003.10:g.49143179del NCBI36
NG_008094.1:g.7426del

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.1035del MANE Select ENSP00000307156.4:p.Lys346SerfsTer24
ENST00000305544.8:c.1035del ENSP00000307156.4:p.Lys346SerfsTer24
ENST00000418109.5:c.1035del ENSP00000388325.1:p.Lys346SerfsTer24
NM_002292.3:c.1035del NP_002283.3:p.Lys346SerfsTer24
XM_005265127.3:c.1035del XP_005265184.1:p.Lys346SerfsTer24
XM_005265127.4:c.1035del XP_005265184.1:p.Lys346SerfsTer24
NM_002292.4:c.1035del MANE Select NP_002283.3:p.Lys346SerfsTer24