Canonical Allele Identifier: CA1346039275
Gene: SYN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12187939C= , CM000665.2:g.12187939C= GRCh38
NC_000003.11:g.12229439C= , CM000665.1:g.12229439C= GRCh37
NC_000003.10:g.12204439C= NCBI36
NG_011728.2:g.188552C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000621198.5:c.1613+327C= MANE Select ENSP00000480050.1:n.1613+327C=
ENST00000439861.5:n.1232+327C=
ENST00000621198.4:c.1613+327C= ENSP00000480050.1:n.1613+327C=
NM_133625.4:c.1613+327C= NP_598328.1:n.1613+327C=
XM_006713312.2:c.1130+327C= XP_006713375.1:n.1130+327C=
XM_006713313.2:c.842+327C= XP_006713376.1:n.842+327C=
XM_006713312.4:c.1130+327C= XP_006713375.1:n.1130+327C=
XM_017007087.1:c.941+327C= XP_016862576.1:n.941+327C=
NM_133625.5:c.1613+327C= NP_598328.1:n.1613+327C=
NM_133625.6:c.1613+327C= MANE Select NP_598328.1:n.1613+327C=
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