Canonical Allele Identifier: CA422578064

Gene: SYT2

Linked Data

• dbSNP Id: rs1690311705
• gnomAD v3: 1-202596760-C-T
• gnomAD v4: 1-202596760-C-T
• MyVariant Identifiers: chr1:g.202565888C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596760C>T , CM000663.2:g.202596760C>T	GRCh38
NC_000001.10:g.202565888C>T , CM000663.1:g.202565888C>T	GRCh37
NC_000001.9:g.200832511C>T	NCBI36
NG_041776.1:g.118664G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1257G>A MANE Select	ENSP00000356237.4:p.Lys419=
ENST00000367267.5:c.1257G>A	ENSP00000356236.1:p.Lys419=
ENST00000367268.4:c.1257G>A	ENSP00000356237.4:p.Lys419=
NM_001136504.1:c.1257G>A	NP_001129976.1:p.Lys419=
NM_177402.4:c.1257G>A	NP_796376.2:p.Lys419=
XM_011509192.1:c.1266G>A	XP_011507494.1:p.Lys422=
XM_011509192.2:c.1266G>A	XP_011507494.1:p.Lys422=
XM_017000309.2:c.1437G>A	XP_016855798.1:p.Lys479=
XM_017000310.2:c.1428G>A	XP_016855799.1:p.Lys476=
XM_017000311.2:c.1266G>A	XP_016855800.1:p.Lys422=
XM_017000312.1:c.1266G>A	XP_016855801.1:p.Lys422=
XM_017000313.1:c.1257G>A	XP_016855802.1:p.Lys419=
NM_177402.5:c.1257G>A MANE Select	NP_796376.2:p.Lys419=