Canonical Allele Identifier: CA70119337
Gene: SYN2 HGNC NCBI

Linked Data

dbSNP Id: rs35152328
gnomAD v2: 3-12229535-A-AT
gnomAD v3: 3-12188035-A-AT
gnomAD v4: 3-12188035-A-AT
MyVariant Identifiers: chr3:g.12229535_12229536insT (hg19) chr3:g.12188035_12188036insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12188040dup , CM000665.2:g.12188040dup GRCh38
NC_000003.11:g.12229540dup , CM000665.1:g.12229540dup GRCh37
NC_000003.10:g.12204540dup NCBI36
NG_011728.2:g.188653dup

Transcript Alleles

HGVS Amino-acid change
ENST00000621198.5:c.1613+428dup MANE Select ENSP00000480050.1:n.1613+428dup
ENST00000439861.5:n.1232+428dup
ENST00000621198.4:c.1613+428dup ENSP00000480050.1:n.1613+428dup
NM_133625.4:c.1613+428dup NP_598328.1:n.1613+428dup
XM_006713312.2:c.1130+428dup XP_006713375.1:n.1130+428dup
XM_006713313.2:c.842+428dup XP_006713376.1:n.842+428dup
XM_006713312.4:c.1130+428dup XP_006713375.1:n.1130+428dup
XM_017007087.1:c.941+428dup XP_016862576.1:n.941+428dup
NM_133625.5:c.1613+428dup NP_598328.1:n.1613+428dup
NM_133625.6:c.1613+428dup MANE Select NP_598328.1:n.1613+428dup
Search 100 bp 5'
Search 100 bp 3'