Canonical Allele Identifier: CA344255641

Gene: SYT2

Linked Data

• dbSNP Id: rs1690312757
• gnomAD v3: 1-202596780-C-T
• gnomAD v4: 1-202596780-C-T
• MyVariant Identifiers: chr1:g.202565908C>T (hg19) ; chr1:g.202596780C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596780C>T , CM000663.2:g.202596780C>T	GRCh38
NC_000001.10:g.202565908C>T , CM000663.1:g.202565908C>T	GRCh37
NC_000001.9:g.200832531C>T	NCBI36
NG_041776.1:g.118644G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1237G>A MANE Select	ENSP00000356237.4:p.Ala413Thr
ENST00000367267.5:c.1237G>A	ENSP00000356236.1:p.Ala413Thr
ENST00000367268.4:c.1237G>A	ENSP00000356237.4:p.Ala413Thr
NM_001136504.1:c.1237G>A	NP_001129976.1:p.Ala413Thr
NM_177402.4:c.1237G>A	NP_796376.2:p.Ala413Thr
XM_011509192.1:c.1246G>A	XP_011507494.1:p.Ala416Thr
XM_011509192.2:c.1246G>A	XP_011507494.1:p.Ala416Thr
XM_017000309.2:c.1417G>A	XP_016855798.1:p.Ala473Thr
XM_017000310.2:c.1408G>A	XP_016855799.1:p.Ala470Thr
XM_017000311.2:c.1246G>A	XP_016855800.1:p.Ala416Thr
XM_017000312.1:c.1246G>A	XP_016855801.1:p.Ala416Thr
XM_017000313.1:c.1237G>A	XP_016855802.1:p.Ala413Thr
NM_177402.5:c.1237G>A MANE Select	NP_796376.2:p.Ala413Thr