Canonical Allele Identifier: CA400861911
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171929T>C (hg19) chr17:g.70175788T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175788T>C , CM000679.2:g.70175788T>C GRCh38
NC_000017.10:g.68171929T>C , CM000679.1:g.68171929T>C GRCh37
NC_000017.9:g.65683524T>C NCBI36
NG_008798.1:g.11254T>C , LRG_328:g.11254T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.749T>C MANE Select ENSP00000243457.2:p.Ile250Thr
ENST00000243457.3:c.749T>C ENSP00000243457.2:p.Ile250Thr
ENST00000535240.1:c.749T>C ENSP00000441848.1:p.Ile250Thr
NM_000891.2:c.749T>C , LRG_328t1:c.749T>C NP_000882.1:p.Ile250Thr
XM_011524779.1:c.749T>C XP_011523081.1:p.Ile250Thr
NM_000891.3:c.749T>C MANE Select NP_000882.1:p.Ile250Thr
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