Canonical Allele Identifier: CA35575399

Gene: SYT2

Linked Data

• dbSNP Id: rs1003439203
• gnomAD v3: 1-202597019-A-G
• gnomAD v4: 1-202597019-A-G
• MyVariant Identifiers: chr1:g.202566147A>G (hg19) ; chr1:g.202597019A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202597019A>G , CM000663.2:g.202597019A>G	GRCh38
NC_000001.10:g.202566147A>G , CM000663.1:g.202566147A>G	GRCh37
NC_000001.9:g.200832770A>G	NCBI36
NG_041776.1:g.118405T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1054-56T>C MANE Select	ENSP00000356237.4:n.1054-56T>C
ENST00000367267.5:c.1054-56T>C	ENSP00000356236.1:n.1054-56T>C
ENST00000367268.4:c.1054-56T>C	ENSP00000356237.4:n.1054-56T>C
NM_001136504.1:c.1054-56T>C	NP_001129976.1:n.1054-56T>C
NM_177402.4:c.1054-56T>C	NP_796376.2:n.1054-56T>C
XM_011509192.1:c.1063-56T>C	XP_011507494.1:n.1063-56T>C
XR_922430.1:n.43A>G
XM_011509192.2:c.1063-56T>C	XP_011507494.1:n.1063-56T>C
XM_017000309.2:c.1234-56T>C	XP_016855798.1:n.1234-56T>C
XM_017000310.2:c.1225-56T>C	XP_016855799.1:n.1225-56T>C
XM_017000311.2:c.1063-56T>C	XP_016855800.1:n.1063-56T>C
XM_017000312.1:c.1063-56T>C	XP_016855801.1:n.1063-56T>C
XM_017000313.1:c.1054-56T>C	XP_016855802.1:n.1054-56T>C
NM_177402.5:c.1054-56T>C MANE Select	NP_796376.2:n.1054-56T>C