Canonical Allele Identifier: CA1045142191

Gene: SYN2

Linked Data

• dbSNP Id: rs1696978163
• gnomAD v3: 3-12140015-C-T
• gnomAD v4: 3-12140015-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12140015C>T , CM000665.2:g.12140015C>T	GRCh38
NC_000003.11:g.12181515C>T , CM000665.1:g.12181515C>T	GRCh37
NC_000003.10:g.12156515C>T	NCBI36
NG_011728.2:g.140628C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.378-636C>T MANE Select	ENSP00000480050.1:n.378-636C>T
ENST00000424884.1:n.127-636C>T
ENST00000620175.4:c.378-636C>T	ENSP00000484916.1:n.378-636C>T
ENST00000621198.4:c.378-636C>T	ENSP00000480050.1:n.378-636C>T
NM_003178.5:c.378-636C>T	NP_003169.2:n.378-636C>T
NM_133625.4:c.378-636C>T	NP_598328.1:n.378-636C>T
XM_006713311.2:c.378-636C>T	XP_006713374.1:n.378-636C>T
XM_006713311.3:c.378-636C>T	XP_006713374.1:n.378-636C>T
XR_001740240.1:n.564-636C>T
NM_133625.5:c.378-636C>T	NP_598328.1:n.378-636C>T
NM_133625.6:c.378-636C>T MANE Select	NP_598328.1:n.378-636C>T
NM_003178.6:c.378-636C>T	NP_003169.2:n.378-636C>T