Canonical Allele Identifier: CA1346018038
Gene: SYN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12140076C= , CM000665.2:g.12140076C= GRCh38
NC_000003.11:g.12181576C= , CM000665.1:g.12181576C= GRCh37
NC_000003.10:g.12156576C= NCBI36
NG_011728.2:g.140689C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000621198.5:c.378-575C= MANE Select ENSP00000480050.1:n.378-575C=
ENST00000424884.1:n.127-575C=
ENST00000620175.4:c.378-575C= ENSP00000484916.1:n.378-575C=
ENST00000621198.4:c.378-575C= ENSP00000480050.1:n.378-575C=
NM_003178.5:c.378-575C= NP_003169.2:n.378-575C=
NM_133625.4:c.378-575C= NP_598328.1:n.378-575C=
XM_006713311.2:c.378-575C= XP_006713374.1:n.378-575C=
XM_006713311.3:c.378-575C= XP_006713374.1:n.378-575C=
XR_001740240.1:n.564-575C=
NM_133625.5:c.378-575C= NP_598328.1:n.378-575C=
NM_133625.6:c.378-575C= MANE Select NP_598328.1:n.378-575C=
NM_003178.6:c.378-575C= NP_003169.2:n.378-575C=
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