Canonical Allele Identifier: CA1346033232

Gene: SYN2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12159406C>G , CM000665.2:g.12159406C>G	GRCh38
NC_000003.11:g.12200906C>G , CM000665.1:g.12200906C>G	GRCh37
NC_000003.10:g.12175906C>G	NCBI36
NG_011728.2:g.160019C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.775-2140C>G MANE Select	ENSP00000480050.1:n.775-2140C>G
ENST00000439861.5:n.226-2140C>G
ENST00000447752.2:n.223+535C>G
ENST00000620175.4:c.775-2140C>G	ENSP00000484916.1:n.775-2140C>G
ENST00000621198.4:c.775-2140C>G	ENSP00000480050.1:n.775-2140C>G
NM_003178.5:c.775-2140C>G	NP_003169.2:n.775-2140C>G
NM_133625.4:c.775-2140C>G	NP_598328.1:n.775-2140C>G
XM_006713311.2:c.775-2140C>G	XP_006713374.1:n.775-2140C>G
XM_006713312.2:c.292-2140C>G	XP_006713375.1:n.292-2140C>G
XM_006713313.2:c.4-2140C>G	XP_006713376.1:n.4-2140C>G
XM_006713311.3:c.775-2140C>G	XP_006713374.1:n.775-2140C>G
XM_006713312.4:c.292-2140C>G	XP_006713375.1:n.292-2140C>G
XM_017007087.1:c.102+815C>G	XP_016862576.1:n.102+815C>G
XR_001740240.1:n.961-2140C>G
NM_133625.5:c.775-2140C>G	NP_598328.1:n.775-2140C>G
NM_133625.6:c.775-2140C>G MANE Select	NP_598328.1:n.775-2140C>G
NM_003178.6:c.775-2140C>G	NP_003169.2:n.775-2140C>G