Canonical Allele Identifier: CA400859772
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171240G>C (hg19) chr17:g.70175099G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175099G>C , CM000679.2:g.70175099G>C GRCh38
NC_000017.10:g.68171240G>C , CM000679.1:g.68171240G>C GRCh37
NC_000017.9:g.65682835G>C NCBI36
NG_008798.1:g.10565G>C , LRG_328:g.10565G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.60G>C MANE Select ENSP00000243457.2:p.Lys20Asn
ENST00000243457.3:c.60G>C ENSP00000243457.2:p.Lys20Asn
ENST00000535240.1:c.60G>C ENSP00000441848.1:p.Lys20Asn
NM_000891.2:c.60G>C , LRG_328t1:c.60G>C NP_000882.1:p.Lys20Asn
XM_011524779.1:c.60G>C XP_011523081.1:p.Lys20Asn
NM_000891.3:c.60G>C MANE Select NP_000882.1:p.Lys20Asn
Search 100 bp 5'
Search 100 bp 3'