Canonical Allele Identifier: CA898007538

Gene: SYN2

Linked Data

• dbSNP Id: rs1382805238
• MyVariant Identifiers: chr3:g.12229436G>C (hg19) ; chr3:g.12187936G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12187936G>C , CM000665.2:g.12187936G>C	GRCh38
NC_000003.11:g.12229436G>C , CM000665.1:g.12229436G>C	GRCh37
NC_000003.10:g.12204436G>C	NCBI36
NG_011728.2:g.188549G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.1613+324G>C MANE Select	ENSP00000480050.1:n.1613+324G>C
ENST00000439861.5:n.1232+324G>C
ENST00000621198.4:c.1613+324G>C	ENSP00000480050.1:n.1613+324G>C
NM_133625.4:c.1613+324G>C	NP_598328.1:n.1613+324G>C
XM_006713312.2:c.1130+324G>C	XP_006713375.1:n.1130+324G>C
XM_006713313.2:c.842+324G>C	XP_006713376.1:n.842+324G>C
XM_006713312.4:c.1130+324G>C	XP_006713375.1:n.1130+324G>C
XM_017007087.1:c.941+324G>C	XP_016862576.1:n.941+324G>C
NM_133625.5:c.1613+324G>C	NP_598328.1:n.1613+324G>C
NM_133625.6:c.1613+324G>C MANE Select	NP_598328.1:n.1613+324G>C