Canonical Allele Identifier: CA398488707
Gene: KCNJ18 HGNC NCBI

Linked Data

dbSNP Id: rs527236152
MyVariant Identifiers: chr17:g.21703205C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.21703205C>A , CM000679.2:g.21703205C>A GRCh38
NG_033093.1:g.15683C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000567955.3:c.419C>A MANE Select ENSP00000457807.2:p.Thr140Lys
NM_001194958.2:c.419C>A MANE Select NP_001181887.2:p.Thr140Lys
XM_005276919.2:c.725C>A XP_005276976.1:p.Thr242Lys
XM_005276919.3:c.725C>A XP_005276976.1:p.Thr242Lys
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