Canonical Allele Identifier: CA400862060
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171964T>A (hg19) chr17:g.70175823T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175823T>A , CM000679.2:g.70175823T>A GRCh38
NC_000017.10:g.68171964T>A , CM000679.1:g.68171964T>A GRCh37
NC_000017.9:g.65683559T>A NCBI36
NG_008798.1:g.11289T>A , LRG_328:g.11289T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.784T>A MANE Select ENSP00000243457.2:p.Phe262Ile
ENST00000243457.3:c.784T>A ENSP00000243457.2:p.Phe262Ile
ENST00000535240.1:c.784T>A ENSP00000441848.1:p.Phe262Ile
NM_000891.2:c.784T>A , LRG_328t1:c.784T>A NP_000882.1:p.Phe262Ile
XM_011524779.1:c.784T>A XP_011523081.1:p.Phe262Ile
NM_000891.3:c.784T>A MANE Select NP_000882.1:p.Phe262Ile
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