Canonical Allele Identifier: CA868372710

Gene: SYK

Linked Data

• dbSNP Id: rs1280139089
• gnomAD v3: 9-90870699-T-C
• gnomAD v4: 9-90870699-T-C
• MyVariant Identifiers: chr9:g.93632981T>C (hg19) ; chr9:g.90870699T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.90870699T>C , CM000671.2:g.90870699T>C	GRCh38
NC_000009.11:g.93632981T>C , CM000671.1:g.93632981T>C	GRCh37
NC_000009.10:g.92672802T>C	NCBI36
NG_017046.1:g.73970T>C
NG_017046.2:g.73970T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375754.9:c.915+3500T>C MANE Select	ENSP00000364907.4:n.915+3500T>C
ENST00000375746.1:c.915+3500T>C	ENSP00000364898.1:n.915+3500T>C
ENST00000375747.5:c.847-3505T>C	ENSP00000364899.1:n.847-3505T>C
ENST00000375751.8:c.847-3505T>C	ENSP00000364904.4:n.847-3505T>C
ENST00000375754.8:c.915+3500T>C	ENSP00000364907.4:n.915+3500T>C
NM_001135052.3:c.847-3505T>C	NP_001128524.1:n.847-3505T>C
NM_001174167.2:c.915+3500T>C	NP_001167638.1:n.915+3500T>C
NM_001174168.2:c.847-3505T>C	NP_001167639.1:n.847-3505T>C
NM_003177.6:c.915+3500T>C	NP_003168.2:n.915+3500T>C
XM_005252147.2:c.915+3500T>C	XP_005252204.1:n.915+3500T>C
XM_011518946.1:c.915+3500T>C	XP_011517248.1:n.915+3500T>C
XM_011518947.1:c.847-3505T>C	XP_011517249.1:n.847-3505T>C
XR_929837.1:n.1118+3463T>C
XM_005252147.4:c.915+3500T>C	XP_005252204.1:n.915+3500T>C
XM_011518946.3:c.915+3500T>C	XP_011517248.1:n.915+3500T>C
XR_001746370.2:n.1118+3463T>C
NM_003177.7:c.915+3500T>C MANE Select	NP_003168.2:n.915+3500T>C
NM_001135052.4:c.847-3505T>C	NP_001128524.1:n.847-3505T>C
NM_001174167.3:c.915+3500T>C	NP_001167638.1:n.915+3500T>C
NM_001174168.3:c.847-3505T>C	NP_001167639.1:n.847-3505T>C