Canonical Allele Identifier: CA2565753829
Gene: SYN2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12140167T>A , CM000665.2:g.12140167T>A GRCh38
NC_000003.11:g.12181667T>A , CM000665.1:g.12181667T>A GRCh37
NC_000003.10:g.12156667T>A NCBI36
NG_011728.2:g.140780T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000621198.5:c.378-484T>A MANE Select ENSP00000480050.1:n.378-484T>A
ENST00000424884.1:n.127-484T>A
ENST00000620175.4:c.378-484T>A ENSP00000484916.1:n.378-484T>A
ENST00000621198.4:c.378-484T>A ENSP00000480050.1:n.378-484T>A
NM_003178.5:c.378-484T>A NP_003169.2:n.378-484T>A
NM_133625.4:c.378-484T>A NP_598328.1:n.378-484T>A
XM_006713311.2:c.378-484T>A XP_006713374.1:n.378-484T>A
XM_006713311.3:c.378-484T>A XP_006713374.1:n.378-484T>A
XR_001740240.1:n.564-484T>A
NM_133625.5:c.378-484T>A NP_598328.1:n.378-484T>A
NM_133625.6:c.378-484T>A MANE Select NP_598328.1:n.378-484T>A
NM_003178.6:c.378-484T>A NP_003169.2:n.378-484T>A
Search 100 bp 5'
Search 100 bp 3'