Canonical Allele Identifier: CA344256096

Gene: SYT2

Linked Data

• MyVariant Identifiers: chr1:g.202566048C>A (hg19) ; chr1:g.202596920C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596920C>A , CM000663.2:g.202596920C>A	GRCh38
NC_000001.10:g.202566048C>A , CM000663.1:g.202566048C>A	GRCh37
NC_000001.9:g.200832671C>A	NCBI36
NG_041776.1:g.118504G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1097G>T MANE Select	ENSP00000356237.4:p.Gly366Val
ENST00000367267.5:c.1097G>T	ENSP00000356236.1:p.Gly366Val
ENST00000367268.4:c.1097G>T	ENSP00000356237.4:p.Gly366Val
NM_001136504.1:c.1097G>T	NP_001129976.1:p.Gly366Val
NM_177402.4:c.1097G>T	NP_796376.2:p.Gly366Val
XM_011509192.1:c.1106G>T	XP_011507494.1:p.Gly369Val
XM_011509192.2:c.1106G>T	XP_011507494.1:p.Gly369Val
XM_017000309.2:c.1277G>T	XP_016855798.1:p.Gly426Val
XM_017000310.2:c.1268G>T	XP_016855799.1:p.Gly423Val
XM_017000311.2:c.1106G>T	XP_016855800.1:p.Gly369Val
XM_017000312.1:c.1106G>T	XP_016855801.1:p.Gly369Val
XM_017000313.1:c.1097G>T	XP_016855802.1:p.Gly366Val
NM_177402.5:c.1097G>T MANE Select	NP_796376.2:p.Gly366Val