Canonical Allele Identifier: CA1025210700

Gene: SYN3

Linked Data

• dbSNP Id: rs2053210186
• gnomAD v3: 22-33006759-T-C
• gnomAD v4: 22-33006759-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.33006759T>C , CM000684.2:g.33006759T>C	GRCh38
NC_000022.10:g.33402744T>C , CM000684.1:g.33402744T>C	GRCh37
NC_000022.9:g.31732744T>C	NCBI36
NG_029545.1:g.56634A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358763.7:c.-97A>G MANE Select	ENSP00000351614.2:n.-97A>G
ENST00000358763.6:c.-97A>G	ENSP00000351614.2:n.-97A>G
ENST00000412575.1:c.-97A>G	ENSP00000388582.1:n.-97A>G
ENST00000441821.5:c.-97A>G	ENSP00000395794.1:n.-97A>G
NM_001135774.1:c.-97A>G	NP_001129246.1:n.-97A>G
NM_003490.3:c.-97A>G	NP_003481.3:n.-97A>G
NM_133633.2:c.-97A>G	NP_598344.2:n.-97A>G
XM_011530405.1:c.-97A>G	XP_011528707.1:n.-97A>G
XM_011530406.1:c.-97A>G	XP_011528708.1:n.-97A>G
XM_011530407.1:c.-97A>G	XP_011528709.1:n.-97A>G
XM_011530408.1:c.-97A>G	XP_011528710.1:n.-97A>G
XM_011530409.1:c.-97A>G	XP_011528711.1:n.-97A>G
XM_011530411.1:c.-97A>G	XP_011528713.1:n.-97A>G
XM_011530413.1:c.-97A>G	XP_011528715.1:n.-97A>G
XM_011530414.1:c.-97A>G	XP_011528716.1:n.-97A>G
XR_937927.1:n.388A>G
XM_011530405.3:c.-97A>G	XP_011528707.1:n.-97A>G
XM_011530406.3:c.-97A>G	XP_011528708.1:n.-97A>G
XM_011530407.3:c.-97A>G	XP_011528709.1:n.-97A>G
XM_011530408.2:c.-97A>G	XP_011528710.1:n.-97A>G
XM_017028961.2:c.-97A>G	XP_016884450.1:n.-97A>G
XM_017028962.2:c.-97A>G	XP_016884451.1:n.-97A>G
XM_017028963.2:c.-97A>G	XP_016884452.1:n.-97A>G
XM_017028964.2:c.-97A>G	XP_016884453.1:n.-97A>G
XR_001755317.2:n.141A>G
NM_001135774.2:c.-97A>G	NP_001129246.1:n.-97A>G
NM_001369907.1:c.-97A>G	NP_001356836.1:n.-97A>G
NM_001369908.1:c.-97A>G	NP_001356837.1:n.-97A>G
NM_001369909.1:c.-97A>G	NP_001356838.1:n.-97A>G
NM_001369910.1:c.-97A>G	NP_001356839.1:n.-97A>G
NM_003490.4:c.-97A>G MANE Select	NP_003481.3:n.-97A>G
NM_133633.3:c.-97A>G	NP_598344.2:n.-97A>G