Canonical Allele Identifier: CA12843739
Gene: STK3 HGNC NCBI

Linked Data

dbSNP Id: rs3019286
gnomAD v2: 8-99895405-G-A
gnomAD v3: 8-98883177-G-A
gnomAD v4: 8-98883177-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98883177G>A , CM000670.2:g.98883177G>A GRCh38
NC_000008.10:g.99895405G>A , CM000670.1:g.99895405G>A GRCh37
NC_000008.9:g.99964581G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000523567.1:n.149+470C>T
ENST00000523601.5:c.110+470C>T ENSP00000429744.1:n.110+470C>T
ENST00000523960.1:n.1054C>T
NM_001256312.1:c.110+470C>T NP_001243241.1:n.110+470C>T
XM_011517247.1:c.110+470C>T XP_011515549.1:n.110+470C>T
XM_011517248.1:c.110+470C>T XP_011515550.1:n.110+470C>T
XM_011517249.1:c.110+470C>T XP_011515551.1:n.110+470C>T
XM_011517250.1:c.110+470C>T XP_011515552.1:n.110+470C>T
XM_011517252.1:c.110+470C>T XP_011515554.1:n.110+470C>T
XM_011517256.1:c.110+470C>T XP_011515558.1:n.110+470C>T
XM_011517257.1:c.110+470C>T XP_011515559.1:n.110+470C>T
XM_011517248.2:c.281+470C>T XP_011515550.2:n.281+470C>T
XM_011517252.3:c.281+470C>T XP_011515554.2:n.281+470C>T
XM_011517257.2:c.281+470C>T XP_011515559.2:n.281+470C>T
XM_017013756.1:c.281+470C>T XP_016869245.1:n.281+470C>T
XM_017013757.1:c.281+470C>T XP_016869246.1:n.281+470C>T
XM_017013762.2:c.281+470C>T XP_016869251.1:n.281+470C>T
XR_001745584.1:n.2140+470C>T
XR_001745585.1:n.2140+470C>T
XR_001745586.1:n.2140+470C>T
NM_001256312.2:c.110+470C>T NP_001243241.1:n.110+470C>T