Canonical Allele Identifier: CA400859925
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171309C>G (hg19) chr17:g.70175168C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175168C>G , CM000679.2:g.70175168C>G GRCh38
NC_000017.10:g.68171309C>G , CM000679.1:g.68171309C>G GRCh37
NC_000017.9:g.65682904C>G NCBI36
NG_008798.1:g.10634C>G , LRG_328:g.10634C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.129C>G MANE Select ENSP00000243457.2:p.Cys43Trp
ENST00000243457.3:c.129C>G ENSP00000243457.2:p.Cys43Trp
ENST00000535240.1:c.129C>G ENSP00000441848.1:p.Cys43Trp
NM_000891.2:c.129C>G , LRG_328t1:c.129C>G NP_000882.1:p.Cys43Trp
XM_011524779.1:c.129C>G XP_011523081.1:p.Cys43Trp
NM_000891.3:c.129C>G MANE Select NP_000882.1:p.Cys43Trp
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