Canonical Allele Identifier: CA1363342659
Gene: LAMB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49130740_49130741delinsTC , CM000665.2:g.49130740_49130741delinsTC GRCh38
NC_000003.11:g.49168173_49168174delinsTC , CM000665.1:g.49168173_49168174delinsTC GRCh37
NC_000003.10:g.49143177_49143178delinsTC NCBI36
NG_008094.1:g.7426_7427delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.1035_1036delinsGA MANE Select ENSP00000307156.4:p.Arg345=
ENST00000305544.8:c.1035_1036delinsGA ENSP00000307156.4:p.Arg345=
ENST00000418109.5:c.1035_1036delinsGA ENSP00000388325.1:p.Arg345=
NM_002292.3:c.1035_1036delinsGA NP_002283.3:p.Arg345=
XM_005265127.3:c.1035_1036delinsGA XP_005265184.1:p.Arg345=
XM_005265127.4:c.1035_1036delinsGA XP_005265184.1:p.Arg345=
NM_002292.4:c.1035_1036delinsGA MANE Select NP_002283.3:p.Arg345=
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