Canonical Allele Identifier: CA1346039294
Gene: SYN2 HGNC NCBI

Linked Data

dbSNP Id: rs1698379593

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12187977C>T , CM000665.2:g.12187977C>T GRCh38
NC_000003.11:g.12229477C>T , CM000665.1:g.12229477C>T GRCh37
NC_000003.10:g.12204477C>T NCBI36
NG_011728.2:g.188590C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000621198.5:c.1613+365C>T MANE Select ENSP00000480050.1:n.1613+365C>T
ENST00000439861.5:n.1232+365C>T
ENST00000621198.4:c.1613+365C>T ENSP00000480050.1:n.1613+365C>T
NM_133625.4:c.1613+365C>T NP_598328.1:n.1613+365C>T
XM_006713312.2:c.1130+365C>T XP_006713375.1:n.1130+365C>T
XM_006713313.2:c.842+365C>T XP_006713376.1:n.842+365C>T
XM_006713312.4:c.1130+365C>T XP_006713375.1:n.1130+365C>T
XM_017007087.1:c.941+365C>T XP_016862576.1:n.941+365C>T
NM_133625.5:c.1613+365C>T NP_598328.1:n.1613+365C>T
NM_133625.6:c.1613+365C>T MANE Select NP_598328.1:n.1613+365C>T