Canonical Allele Identifier: CA37763320

Gene: KCNK2

Linked Data

• dbSNP Id: rs1048493206
• MyVariant Identifiers: chr1:g.215362298G>T (hg19) ; chr1:g.215188955G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215188955G>T , CM000663.2:g.215188955G>T	GRCh38
NC_000001.10:g.215362298G>T , CM000663.1:g.215362298G>T	GRCh37
NC_000001.9:g.213428921G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000444842.7:c.824-5998G>T MANE Select	ENSP00000394033.2:n.824-5998G>T
ENST00000391894.6:c.779-5998G>T	ENSP00000375764.2:n.779-5998G>T
ENST00000391895.6:c.812-5998G>T	ENSP00000375765.2:n.812-5998G>T
ENST00000444842.6:c.824-5998G>T	ENSP00000394033.2:n.824-5998G>T
ENST00000467031.5:c.625-5998G>T	ENSP00000420203.1:n.625-5998G>T
ENST00000470177.5:c.*235-5998G>T	ENSP00000419633.1:n.*235-5998G>T
ENST00000474771.5:c.592-5998G>T	ENSP00000420499.1:n.592-5998G>T
ENST00000486921.5:c.*235-5998G>T	ENSP00000418706.1:n.*235-5998G>T
NM_001017424.2:c.812-5998G>T	NP_001017424.1:n.812-5998G>T
NM_001017425.2:c.824-5998G>T	NP_001017425.2:n.824-5998G>T
NM_014217.3:c.779-5998G>T	NP_055032.1:n.779-5998G>T
XM_011509521.1:c.782-5998G>T	XP_011507823.1:n.782-5998G>T
XM_011509522.1:c.656-5998G>T	XP_011507824.1:n.656-5998G>T
XM_011509523.1:c.656-5998G>T	XP_011507825.1:n.656-5998G>T
XM_011509524.1:c.656-5998G>T	XP_011507826.1:n.656-5998G>T
XR_922594.1:n.182+1646C>A
XM_011509522.2:c.656-5998G>T	XP_011507824.1:n.656-5998G>T
XM_011509524.2:c.656-5998G>T	XP_011507826.1:n.656-5998G>T
XM_017001248.1:c.812-5998G>T	XP_016856737.1:n.812-5998G>T
XM_017001249.1:c.782-5998G>T	XP_016856738.1:n.782-5998G>T
NM_001017424.3:c.812-5998G>T	NP_001017424.1:n.812-5998G>T
NM_001017425.3:c.824-5998G>T MANE Select	NP_001017425.2:n.824-5998G>T
NM_014217.4:c.779-5998G>T	NP_055032.1:n.779-5998G>T