Canonical Allele Identifier: CA2665695203
Gene: LAMB2 HGNC NCBI

Linked Data

gnomAD v4: 3-49122836-G-GAGA
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49122838_49122839insAAG , CM000665.2:g.49122838_49122839insAAG GRCh38
NC_000003.11:g.49160271_49160272insAAG , CM000665.1:g.49160271_49160272insAAG GRCh37
NC_000003.10:g.49135275_49135276insAAG NCBI36
NG_008094.1:g.15330_15331insTCT
NG_054716.1:g.3102_3103insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.4440_4441insTCT MANE Select ENSP00000307156.4:p.Thr1480_Arg1481insSer
ENST00000305544.8:c.4440_4441insTCT ENSP00000307156.4:p.Thr1480_Arg1481insSer
ENST00000418109.5:c.4440_4441insTCT ENSP00000388325.1:p.Thr1480_Arg1481insSer
ENST00000469665.1:n.749_750insTCT
NM_002292.3:c.4440_4441insTCT NP_002283.3:p.Thr1480_Arg1481insSer
XM_005265127.3:c.4440_4441insTCT XP_005265184.1:p.Thr1480_Arg1481insSer
XM_005265127.4:c.4440_4441insTCT XP_005265184.1:p.Thr1480_Arg1481insSer
NM_002292.4:c.4440_4441insTCT MANE Select NP_002283.3:p.Thr1480_Arg1481insSer
Search 100 bp 5'
Search 100 bp 3'