Canonical Allele Identifier: CA13033912
Gene: SYK HGNC NCBI
COSMIC:
COSN14849229 (not active)
MyVariant.info:
GRCh38 chr9:g.90865745A>G
GRCh37 chr9:g.93628027A>G
gnomAD v2:
9:93628027 A / G
gnomAD v3:
9:90865745 A / G
gnomAD v4:
chr9-90865745-A-G
Joint Max Group AF 0.25449884 (EAS)
Genomes Max Group AF 0.25449884 (EAS)
dbSNP:
2991216
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.90865745A>G , CM000671.2:g.90865745A>G GRCh38
NC_000009.11:g.93628027A>G , CM000671.1:g.93628027A>G GRCh37
NC_000009.10:g.92667848A>G NCBI36
NG_017046.1:g.69016A>G
NG_017046.2:g.69016A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375754.9:c.846+648A>G MANE Select ENSP00000364907.4:n.846+648A>G
ENST00000375746.1:c.846+648A>G ENSP00000364898.1:n.846+648A>G
ENST00000375747.5:c.846+648A>G ENSP00000364899.1:n.846+648A>G
ENST00000375751.8:c.846+648A>G ENSP00000364904.4:n.846+648A>G
ENST00000375754.8:c.846+648A>G ENSP00000364907.4:n.846+648A>G
NM_001135052.3:c.846+648A>G NP_001128524.1:n.846+648A>G
NM_001174167.2:c.846+648A>G NP_001167638.1:n.846+648A>G
NM_001174168.2:c.846+648A>G NP_001167639.1:n.846+648A>G
NM_003177.6:c.846+648A>G NP_003168.2:n.846+648A>G
XM_005252147.2:c.846+648A>G XP_005252204.1:n.846+648A>G
XM_011518946.1:c.846+648A>G XP_011517248.1:n.846+648A>G
XM_011518947.1:c.846+648A>G XP_011517249.1:n.846+648A>G
XR_929837.1:n.1012+648A>G
XM_005252147.4:c.846+648A>G XP_005252204.1:n.846+648A>G
XM_011518946.3:c.846+648A>G XP_011517248.1:n.846+648A>G
XR_001746370.2:n.1012+648A>G
NM_003177.7:c.846+648A>G MANE Select NP_003168.2:n.846+648A>G
NM_001135052.4:c.846+648A>G NP_001128524.1:n.846+648A>G
NM_001174167.3:c.846+648A>G NP_001167638.1:n.846+648A>G
NM_001174168.3:c.846+648A>G NP_001167639.1:n.846+648A>G
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