Canonical Allele Identifier: CA1346039274
Gene: SYN2 HGNC NCBI

Linked Data

dbSNP Id: rs1382805238
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12187936G>A , CM000665.2:g.12187936G>A GRCh38
NC_000003.11:g.12229436G>A , CM000665.1:g.12229436G>A GRCh37
NC_000003.10:g.12204436G>A NCBI36
NG_011728.2:g.188549G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000621198.5:c.1613+324G>A MANE Select ENSP00000480050.1:n.1613+324G>A
ENST00000439861.5:n.1232+324G>A
ENST00000621198.4:c.1613+324G>A ENSP00000480050.1:n.1613+324G>A
NM_133625.4:c.1613+324G>A NP_598328.1:n.1613+324G>A
XM_006713312.2:c.1130+324G>A XP_006713375.1:n.1130+324G>A
XM_006713313.2:c.842+324G>A XP_006713376.1:n.842+324G>A
XM_006713312.4:c.1130+324G>A XP_006713375.1:n.1130+324G>A
XM_017007087.1:c.941+324G>A XP_016862576.1:n.941+324G>A
NM_133625.5:c.1613+324G>A NP_598328.1:n.1613+324G>A
NM_133625.6:c.1613+324G>A MANE Select NP_598328.1:n.1613+324G>A
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