Canonical Allele Identifier: CA1333610
Gene: SYT2 HGNC NCBI

Linked Data

dbSNP Id: rs777807674

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596963T>C , CM000663.2:g.202596963T>C GRCh38
NC_000001.10:g.202566091T>C , CM000663.1:g.202566091T>C GRCh37
NC_000001.9:g.200832714T>C NCBI36
NG_041776.1:g.118461A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367268.5:c.1054A>G MANE Select ENSP00000356237.4:p.Lys352Glu
ENST00000367267.5:c.1054A>G ENSP00000356236.1:p.Lys352Glu
ENST00000367268.4:c.1054A>G ENSP00000356237.4:p.Lys352Glu
NM_001136504.1:c.1054A>G NP_001129976.1:p.Lys352Glu
NM_177402.4:c.1054A>G NP_796376.2:p.Lys352Glu
XM_011509192.1:c.1063A>G XP_011507494.1:p.Lys355Glu
XM_011509192.2:c.1063A>G XP_011507494.1:p.Lys355Glu
XM_017000309.2:c.1234A>G XP_016855798.1:p.Lys412Glu
XM_017000310.2:c.1225A>G XP_016855799.1:p.Lys409Glu
XM_017000311.2:c.1063A>G XP_016855800.1:p.Lys355Glu
XM_017000312.1:c.1063A>G XP_016855801.1:p.Lys355Glu
XM_017000313.1:c.1054A>G XP_016855802.1:p.Lys352Glu
NM_177402.5:c.1054A>G MANE Select NP_796376.2:p.Lys352Glu