Canonical Allele Identifier: CA1346039286

Gene: SYN2

Linked Data

• dbSNP Id: rs1559461104

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12187957T>G , CM000665.2:g.12187957T>G	GRCh38
NC_000003.11:g.12229457T>G , CM000665.1:g.12229457T>G	GRCh37
NC_000003.10:g.12204457T>G	NCBI36
NG_011728.2:g.188570T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.1613+345T>G MANE Select	ENSP00000480050.1:n.1613+345T>G
ENST00000439861.5:n.1232+345T>G
ENST00000621198.4:c.1613+345T>G	ENSP00000480050.1:n.1613+345T>G
NM_133625.4:c.1613+345T>G	NP_598328.1:n.1613+345T>G
XM_006713312.2:c.1130+345T>G	XP_006713375.1:n.1130+345T>G
XM_006713313.2:c.842+345T>G	XP_006713376.1:n.842+345T>G
XM_006713312.4:c.1130+345T>G	XP_006713375.1:n.1130+345T>G
XM_017007087.1:c.941+345T>G	XP_016862576.1:n.941+345T>G
NM_133625.5:c.1613+345T>G	NP_598328.1:n.1613+345T>G
NM_133625.6:c.1613+345T>G MANE Select	NP_598328.1:n.1613+345T>G