Canonical Allele Identifier: CA15592932
Gene: SYK HGNC NCBI

Linked Data

dbSNP Id: rs1000735

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.90892334C>G , CM000671.2:g.90892334C>G GRCh38
NC_000009.11:g.93654616C>G , CM000671.1:g.93654616C>G GRCh37
NC_000009.10:g.92694437C>G NCBI36
NG_017046.1:g.95605C>G
NG_017046.2:g.95605C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375746.1:c.1836-3194C>G ENSP00000364898.1:p.=
ENST00000375747.5:c.1767-3194C>G ENSP00000364899.1:p.=
ENST00000375751.8:c.1767-3194C>G ENSP00000364904.4:p.=
ENST00000375754.8:c.1836-3194C>G ENSP00000364907.4:p.=
NM_001135052.3:c.1767-3194C>G NP_001128524.1:p.=
NM_001174167.2:c.1836-3194C>G NP_001167638.1:p.=
NM_001174168.2:c.1767-3194C>G NP_001167639.1:p.=
NM_003177.6:c.1836-3194C>G NP_003168.2:p.=
XM_005252147.2:c.1836-3194C>G XP_005252204.1:p.=
XM_011518946.1:c.1836-3194C>G XP_011517248.1:p.=
XM_011518947.1:c.1767-3194C>G XP_011517249.1:p.=
XM_005252147.4:c.1836-3194C>G XP_005252204.1:p.=
XM_011518946.3:c.1836-3194C>G XP_011517248.1:p.=
NM_003177.7:c.1836-3194C>G MANE Select NP_003168.2:p.=
NM_001135052.4:c.1767-3194C>G NP_001128524.1:p.=
NM_001174167.3:c.1836-3194C>G NP_001167638.1:p.=
NM_001174168.3:c.1767-3194C>G NP_001167639.1:p.=