Canonical Allele Identifier: CA730216617

Gene: SYT2

Linked Data

• dbSNP Id: rs763536534
• MyVariant Identifiers: chr1:g.202566113G>C (hg19) ; chr1:g.202596985G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596985G>C , CM000663.2:g.202596985G>C	GRCh38
NC_000001.10:g.202566113G>C , CM000663.1:g.202566113G>C	GRCh37
NC_000001.9:g.200832736G>C	NCBI36
NG_041776.1:g.118439C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1054-22C>G MANE Select	ENSP00000356237.4:n.1054-22C>G
ENST00000367267.5:c.1054-22C>G	ENSP00000356236.1:n.1054-22C>G
ENST00000367268.4:c.1054-22C>G	ENSP00000356237.4:n.1054-22C>G
NM_001136504.1:c.1054-22C>G	NP_001129976.1:n.1054-22C>G
NM_177402.4:c.1054-22C>G	NP_796376.2:n.1054-22C>G
XM_011509192.1:c.1063-22C>G	XP_011507494.1:n.1063-22C>G
XR_922430.1:n.9G>C
XM_011509192.2:c.1063-22C>G	XP_011507494.1:n.1063-22C>G
XM_017000309.2:c.1234-22C>G	XP_016855798.1:n.1234-22C>G
XM_017000310.2:c.1225-22C>G	XP_016855799.1:n.1225-22C>G
XM_017000311.2:c.1063-22C>G	XP_016855800.1:n.1063-22C>G
XM_017000312.1:c.1063-22C>G	XP_016855801.1:n.1063-22C>G
XM_017000313.1:c.1054-22C>G	XP_016855802.1:n.1054-22C>G
NM_177402.5:c.1054-22C>G MANE Select	NP_796376.2:n.1054-22C>G