Canonical Allele Identifier: CA37763303
Gene: KCNK2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10494994

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215188864G>A , CM000663.2:g.215188864G>A GRCh38
NC_000001.10:g.215362207G>A , CM000663.1:g.215362207G>A GRCh37
NC_000001.9:g.213428830G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001017424.2:c.812-6089G>A VV NP_001017424.1:p.=
NM_001017425.2:c.824-6089G>A VV NP_001017425.2:p.=
NM_014217.3:c.779-6089G>A VV NP_055032.1:p.=
XM_011509521.1:c.782-6089G>A XP_011507823.1:p.=
XM_011509522.1:c.656-6089G>A XP_011507824.1:p.=
XM_011509523.1:c.656-6089G>A XP_011507825.1:p.=
XM_011509524.1:c.656-6089G>A XP_011507826.1:p.=
XR_922594.1:n.182+1737C>T
XM_011509522.2:c.656-6089G>A
XM_011509524.2:c.656-6089G>A
XM_017001248.1:c.812-6089G>A XP_016856737.1:p.=
XM_017001249.1:c.782-6089G>A XP_016856738.1:p.=
ENST00000391894.6:c.779-6089G>A ENSP00000375764.2:p.=
ENST00000391895.6:c.812-6089G>A ENSP00000375765.2:p.=
ENST00000444842.6:c.824-6089G>A ENSP00000394033.2:p.=
ENST00000467031.5:c.625-6089G>A ENSP00000420203.1:p.=
ENST00000470177.5:c.*235-6089G>A ENSP00000419633.1:p.=
ENST00000474771.5:c.592-6089G>A ENSP00000420499.1:p.=
ENST00000486921.5:c.*235-6089G>A ENSP00000418706.1:p.=