Canonical Allele Identifier: CA11397642

Gene: SYN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12167171G>T , CM000665.2:g.12167171G>T	GRCh38
NC_000003.11:g.12208671G>T , CM000665.1:g.12208671G>T	GRCh37
NC_000003.10:g.12183671G>T	NCBI36
NG_011728.2:g.167784G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.981-63G>T MANE Select	ENSP00000480050.1:n.981-63G>T
ENST00000425297.2:c.208-63G>T
ENST00000439861.5:n.600-63G>T
ENST00000447752.2:n.430-63G>T
ENST00000620175.4:c.981-63G>T	ENSP00000484916.1:n.981-63G>T
ENST00000621198.4:c.981-63G>T	ENSP00000480050.1:n.981-63G>T
NM_003178.5:c.981-63G>T	NP_003169.2:n.981-63G>T
NM_133625.4:c.981-63G>T	NP_598328.1:n.981-63G>T
XM_006713311.2:c.981-63G>T	XP_006713374.1:n.981-63G>T
XM_006713312.2:c.498-63G>T	XP_006713375.1:n.498-63G>T
XM_006713313.2:c.210-63G>T	XP_006713376.1:n.210-63G>T
XM_006713311.3:c.981-63G>T	XP_006713374.1:n.981-63G>T
XM_006713312.4:c.498-63G>T	XP_006713375.1:n.498-63G>T
XM_017007087.1:c.309-63G>T	XP_016862576.1:n.309-63G>T
XR_001740240.1:n.1335-63G>T
NM_133625.5:c.981-63G>T	NP_598328.1:n.981-63G>T
NM_133625.6:c.981-63G>T MANE Select	NP_598328.1:n.981-63G>T
NM_003178.6:c.981-63G>T	NP_003169.2:n.981-63G>T