Canonical Allele Identifier: CA2840278698
Gene: LAMB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49130801dup , CM000665.2:g.49130801dup GRCh38
NC_000003.11:g.49168234dup , CM000665.1:g.49168234dup GRCh37
NC_000003.10:g.49143238dup NCBI36
NG_008094.1:g.7367dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.976dup MANE Select ENSP00000307156.4:p.Asp326GlyfsTer5
ENST00000305544.8:c.976dup ENSP00000307156.4:p.Asp326GlyfsTer5
ENST00000418109.5:c.976dup ENSP00000388325.1:p.Asp326GlyfsTer5
NM_002292.3:c.976dup NP_002283.3:p.Asp326GlyfsTer5
XM_005265127.3:c.976dup XP_005265184.1:p.Asp326GlyfsTer5
XM_005265127.4:c.976dup XP_005265184.1:p.Asp326GlyfsTer5
NM_002292.4:c.976dup MANE Select NP_002283.3:p.Asp326GlyfsTer5
Search 100 bp 5'
Search 100 bp 3'