Canonical Allele Identifier: CA2566646505
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131132_49131137del , CM000665.2:g.49131132_49131137del GRCh38
NC_000003.11:g.49168565_49168570del , CM000665.1:g.49168565_49168570del GRCh37
NC_000003.10:g.49143569_49143574del NCBI36
NG_008094.1:g.7030_7035del

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.728_733del MANE Select ENSP00000307156.4:p.Thr243_Leu245delinsIl...
ENST00000305544.8:c.728_733del ENSP00000307156.4:p.Thr243_Leu245delinsIl...
ENST00000418109.5:c.728_733del ENSP00000388325.1:p.Thr243_Leu245delinsIl...
ENST00000494831.1:c.281_286del ENSP00000444751.1:p.Thr94_Leu96delinsIle
NM_002292.3:c.728_733del NP_002283.3:p.Thr243_Leu245delinsIle
XM_005265127.3:c.728_733del XP_005265184.1:p.Thr243_Leu245delinsIle
XM_005265127.4:c.728_733del XP_005265184.1:p.Thr243_Leu245delinsIle
NM_002292.4:c.728_733del MANE Select NP_002283.3:p.Thr243_Leu245delinsIle