Canonical Allele Identifier: CA1346017968
Gene: SYN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12139941T= , CM000665.2:g.12139941T= GRCh38
NC_000003.11:g.12181441T= , CM000665.1:g.12181441T= GRCh37
NC_000003.10:g.12156441T= NCBI36
NG_011728.2:g.140554T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000621198.5:c.378-710T= MANE Select ENSP00000480050.1:n.378-710T=
ENST00000424884.1:n.127-710T=
ENST00000620175.4:c.378-710T= ENSP00000484916.1:n.378-710T=
ENST00000621198.4:c.378-710T= ENSP00000480050.1:n.378-710T=
NM_003178.5:c.378-710T= NP_003169.2:n.378-710T=
NM_133625.4:c.378-710T= NP_598328.1:n.378-710T=
XM_006713311.2:c.378-710T= XP_006713374.1:n.378-710T=
XM_006713311.3:c.378-710T= XP_006713374.1:n.378-710T=
XR_001740240.1:n.564-710T=
NM_133625.5:c.378-710T= NP_598328.1:n.378-710T=
NM_133625.6:c.378-710T= MANE Select NP_598328.1:n.378-710T=
NM_003178.6:c.378-710T= NP_003169.2:n.378-710T=
Search 100 bp 5'
Search 100 bp 3'