Canonical Allele Identifier: CA37720440

Gene: KCNK2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215013629G>A , CM000663.2:g.215013629G>A	GRCh38
NC_000001.10:g.215186972G>A , CM000663.1:g.215186972G>A	GRCh37
NC_000001.9:g.213253595G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391895.6:c.34+7674G>A	ENSP00000375765.2:n.34+7674G>A
ENST00000467031.5:c.34+7674G>A	ENSP00000420203.1:n.34+7674G>A
ENST00000486921.5:c.34+7674G>A	ENSP00000418706.1:n.34+7674G>A
NM_001017424.2:c.34+7674G>A	NP_001017424.1:n.34+7674G>A
XM_011509521.1:c.-85+7674G>A	XP_011507823.1:n.-85+7674G>A
XM_017001248.1:c.34+7674G>A	XP_016856737.1:n.34+7674G>A
XM_017001249.1:c.-85+7674G>A	XP_016856738.1:n.-85+7674G>A
NM_001017424.3:c.34+7674G>A	NP_001017424.1:n.34+7674G>A