Canonical Allele Identifier: CA583819151

Gene: STK3

Linked Data

• dbSNP Id: rs1452828160
• gnomAD v2: 8-99895316-T-C
• gnomAD v3: 8-98883088-T-C
• gnomAD v4: 8-98883088-T-C
• MyVariant Identifiers: chr8:g.99895316T>C (hg19) ; chr8:g.98883088T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.98883088T>C , CM000670.2:g.98883088T>C	GRCh38
NC_000008.10:g.99895316T>C , CM000670.1:g.99895316T>C	GRCh37
NC_000008.9:g.99964492T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000523567.1:n.149+559A>G
ENST00000523601.5:c.110+559A>G	ENSP00000429744.1:n.110+559A>G
ENST00000523960.1:n.1143A>G
NM_001256312.1:c.110+559A>G	NP_001243241.1:n.110+559A>G
XM_011517247.1:c.110+559A>G	XP_011515549.1:n.110+559A>G
XM_011517248.1:c.110+559A>G	XP_011515550.1:n.110+559A>G
XM_011517249.1:c.110+559A>G	XP_011515551.1:n.110+559A>G
XM_011517250.1:c.110+559A>G	XP_011515552.1:n.110+559A>G
XM_011517252.1:c.110+559A>G	XP_011515554.1:n.110+559A>G
XM_011517256.1:c.110+559A>G	XP_011515558.1:n.110+559A>G
XM_011517257.1:c.110+559A>G	XP_011515559.1:n.110+559A>G
XM_011517248.2:c.281+559A>G	XP_011515550.2:n.281+559A>G
XM_011517252.3:c.281+559A>G	XP_011515554.2:n.281+559A>G
XM_011517257.2:c.281+559A>G	XP_011515559.2:n.281+559A>G
XM_017013756.1:c.281+559A>G	XP_016869245.1:n.281+559A>G
XM_017013757.1:c.281+559A>G	XP_016869246.1:n.281+559A>G
XM_017013762.2:c.281+559A>G	XP_016869251.1:n.281+559A>G
XR_001745584.1:n.2140+559A>G
XR_001745585.1:n.2140+559A>G
XR_001745586.1:n.2140+559A>G
NM_001256312.2:c.110+559A>G	NP_001243241.1:n.110+559A>G