Canonical Allele Identifier: CA1405859376
Gene: CLSTN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.139963148A= , CM000665.2:g.139963148A= GRCh38
NC_000003.11:g.139681990A= , CM000665.1:g.139681990A= GRCh37
NC_000003.10:g.141164680A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000458420.7:c.109+27665A= MANE Select ENSP00000402460.2:n.109+27665A=
ENST00000511524.1:n.297+27665A=
NM_022131.2:c.109+27665A= NP_071414.2:n.109+27665A=
NM_022131.3:c.109+27665A= MANE Select NP_071414.2:n.109+27665A=
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