Canonical Allele Identifier: CA2481403161
Gene: SYT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596943G= , CM000663.2:g.202596943G= GRCh38
NC_000001.10:g.202566071G= , CM000663.1:g.202566071G= GRCh37
NC_000001.9:g.200832694G= NCBI36
NG_041776.1:g.118481C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367268.5:c.1074C= MANE Select ENSP00000356237.4:p.Thr358=
ENST00000367267.5:c.1074C= ENSP00000356236.1:p.Thr358=
ENST00000367268.4:c.1074C= ENSP00000356237.4:p.Thr358=
NM_001136504.1:c.1074C= NP_001129976.1:p.Thr358=
NM_177402.4:c.1074C= NP_796376.2:p.Thr358=
XM_011509192.1:c.1083C= XP_011507494.1:p.Thr361=
XM_011509192.2:c.1083C= XP_011507494.1:p.Thr361=
XM_017000309.2:c.1254C= XP_016855798.1:p.Thr418=
XM_017000310.2:c.1245C= XP_016855799.1:p.Thr415=
XM_017000311.2:c.1083C= XP_016855800.1:p.Thr361=
XM_017000312.1:c.1083C= XP_016855801.1:p.Thr361=
XM_017000313.1:c.1074C= XP_016855802.1:p.Thr358=
NM_177402.5:c.1074C= MANE Select NP_796376.2:p.Thr358=