Canonical Allele Identifier: CA84590526
Gene: CLSTN2 HGNC NCBI

Linked Data

dbSNP Id: rs927825059
gnomAD v2: 3-140175399-C-T
gnomAD v3: 3-140456557-C-T
gnomAD v4: 3-140456557-C-T
MyVariant Identifiers: chr3:g.140175399C>T (hg19) chr3:g.140456557C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140456557C>T , CM000665.2:g.140456557C>T GRCh38
NC_000003.11:g.140175399C>T , CM000665.1:g.140175399C>T GRCh37
NC_000003.10:g.141658089C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000458420.7:c.974-2964C>T MANE Select ENSP00000402460.2:n.974-2964C>T
ENST00000511524.1:n.1162-2964C>T
ENST00000620185.1:c.782-2964C>T ENSP00000478883.1:n.782-2964C>T
NM_022131.2:c.974-2964C>T NP_071414.2:n.974-2964C>T
XR_924548.1:n.49-1804G>A
XR_924549.1:n.49-1804G>A
XM_017007022.2:c.899-2964C>T XP_016862511.1:n.899-2964C>T
XR_924548.2:n.1503-1804G>A
XR_924549.2:n.1503-1804G>A
NM_022131.3:c.974-2964C>T MANE Select NP_071414.2:n.974-2964C>T
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