Canonical Allele Identifier: CA1345967171

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12022950T= , CM000665.2:g.12022950T=	GRCh38
NC_000003.11:g.12064450T= , CM000665.1:g.12064450T=	GRCh37
NC_000003.10:g.12039450T=	NCBI36
NG_011728.2:g.23563T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000621198.5:c.377+18022T= MANE Select	ENSP00000480050.1:n.377+18022T=
ENST00000620175.4:c.377+18022T=	ENSP00000484916.1:n.377+18022T=
ENST00000621198.4:c.377+18022T=	ENSP00000480050.1:n.377+18022T=
NM_003178.5:c.377+18022T=	NP_003169.2:n.377+18022T=
NM_133625.4:c.377+18022T=	NP_598328.1:n.377+18022T=
XM_006713311.2:c.377+18022T=	XP_006713374.1:n.377+18022T=
XM_006713311.3:c.377+18022T=	XP_006713374.1:n.377+18022T=
XR_001740240.1:n.563+18022T=
NM_133625.5:c.377+18022T=	NP_598328.1:n.377+18022T=
NM_133625.6:c.377+18022T= MANE Select	NP_598328.1:n.377+18022T=
NM_003178.6:c.377+18022T=	NP_003169.2:n.377+18022T=