Canonical Allele Identifier: CA400859790

Gene: KCNJ2

Linked Data

• MyVariant Identifiers: chr17:g.68171248C>T (hg19) ; chr17:g.70175107C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.70175107C>T , CM000679.2:g.70175107C>T	GRCh38
NC_000017.10:g.68171248C>T , CM000679.1:g.68171248C>T	GRCh37
NC_000017.9:g.65682843C>T	NCBI36
NG_008798.1:g.10573C>T , LRG_328:g.10573C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000243457.4:c.68C>T MANE Select	ENSP00000243457.2:p.Thr23Ile
ENST00000243457.3:c.68C>T	ENSP00000243457.2:p.Thr23Ile
ENST00000535240.1:c.68C>T	ENSP00000441848.1:p.Thr23Ile
NM_000891.2:c.68C>T , LRG_328t1:c.68C>T	NP_000882.1:p.Thr23Ile
XM_011524779.1:c.68C>T	XP_011523081.1:p.Thr23Ile
NM_000891.3:c.68C>T MANE Select	NP_000882.1:p.Thr23Ile