Canonical Allele Identifier: CA1346039223

Gene: SYN2

Linked Data

• dbSNP Id: rs1698376520

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12187828G>A , CM000665.2:g.12187828G>A	GRCh38
NC_000003.11:g.12229328G>A , CM000665.1:g.12229328G>A	GRCh37
NC_000003.10:g.12204328G>A	NCBI36
NG_011728.2:g.188441G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.1613+216G>A MANE Select	ENSP00000480050.1:n.1613+216G>A
ENST00000439861.5:n.1232+216G>A
ENST00000621198.4:c.1613+216G>A	ENSP00000480050.1:n.1613+216G>A
NM_133625.4:c.1613+216G>A	NP_598328.1:n.1613+216G>A
XM_006713312.2:c.1130+216G>A	XP_006713375.1:n.1130+216G>A
XM_006713313.2:c.842+216G>A	XP_006713376.1:n.842+216G>A
XM_006713312.4:c.1130+216G>A	XP_006713375.1:n.1130+216G>A
XM_017007087.1:c.941+216G>A	XP_016862576.1:n.941+216G>A
NM_133625.5:c.1613+216G>A	NP_598328.1:n.1613+216G>A
NM_133625.6:c.1613+216G>A MANE Select	NP_598328.1:n.1613+216G>A