Canonical Allele Identifier: CA84565779
Gene: CLSTN2 HGNC NCBI

Linked Data

dbSNP Id: rs17411949
gnomAD v2: 3-140099693-C-T
gnomAD v3: 3-140380851-C-T
gnomAD v4: 3-140380851-C-T
MyVariant Identifiers: chr3:g.140099693C>T (hg19) chr3:g.140380851C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140380851C>T , CM000665.2:g.140380851C>T GRCh38
NC_000003.11:g.140099693C>T , CM000665.1:g.140099693C>T GRCh37
NC_000003.10:g.141582383C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000458420.7:c.233-22778C>T MANE Select ENSP00000402460.2:n.233-22778C>T
ENST00000511524.1:n.421-22778C>T
NM_022131.2:c.233-22778C>T NP_071414.2:n.233-22778C>T
XM_017007022.2:c.158-22778C>T XP_016862511.1:n.158-22778C>T
NM_022131.3:c.233-22778C>T MANE Select NP_071414.2:n.233-22778C>T
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