Canonical Allele Identifier: CA1346018030
Gene: SYN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12140062G= , CM000665.2:g.12140062G= GRCh38
NC_000003.11:g.12181562G= , CM000665.1:g.12181562G= GRCh37
NC_000003.10:g.12156562G= NCBI36
NG_011728.2:g.140675G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000621198.5:c.378-589G= MANE Select ENSP00000480050.1:n.378-589G=
ENST00000424884.1:n.127-589G=
ENST00000620175.4:c.378-589G= ENSP00000484916.1:n.378-589G=
ENST00000621198.4:c.378-589G= ENSP00000480050.1:n.378-589G=
NM_003178.5:c.378-589G= NP_003169.2:n.378-589G=
NM_133625.4:c.378-589G= NP_598328.1:n.378-589G=
XM_006713311.2:c.378-589G= XP_006713374.1:n.378-589G=
XM_006713311.3:c.378-589G= XP_006713374.1:n.378-589G=
XR_001740240.1:n.564-589G=
NM_133625.5:c.378-589G= NP_598328.1:n.378-589G=
NM_133625.6:c.378-589G= MANE Select NP_598328.1:n.378-589G=
NM_003178.6:c.378-589G= NP_003169.2:n.378-589G=
Search 100 bp 5'
Search 100 bp 3'