Canonical Allele Identifier: CA1333608
Gene: SYT2 HGNC NCBI

Linked Data

dbSNP Id: rs749174583

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596944G>T , CM000663.2:g.202596944G>T GRCh38
NC_000001.10:g.202566072G>T , CM000663.1:g.202566072G>T GRCh37
NC_000001.9:g.200832695G>T NCBI36
NG_041776.1:g.118480C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367268.5:c.1073C>A MANE Select ENSP00000356237.4:p.Thr358Asn
ENST00000367267.5:c.1073C>A ENSP00000356236.1:p.Thr358Asn
ENST00000367268.4:c.1073C>A ENSP00000356237.4:p.Thr358Asn
NM_001136504.1:c.1073C>A NP_001129976.1:p.Thr358Asn
NM_177402.4:c.1073C>A NP_796376.2:p.Thr358Asn
XM_011509192.1:c.1082C>A XP_011507494.1:p.Thr361Asn
XM_011509192.2:c.1082C>A XP_011507494.1:p.Thr361Asn
XM_017000309.2:c.1253C>A XP_016855798.1:p.Thr418Asn
XM_017000310.2:c.1244C>A XP_016855799.1:p.Thr415Asn
XM_017000311.2:c.1082C>A XP_016855800.1:p.Thr361Asn
XM_017000312.1:c.1082C>A XP_016855801.1:p.Thr361Asn
XM_017000313.1:c.1073C>A XP_016855802.1:p.Thr358Asn
NM_177402.5:c.1073C>A MANE Select NP_796376.2:p.Thr358Asn