Canonical Allele Identifier: CA351121696
Gene: KCNE4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.223918051A>G (hg19) chr2:g.223053333A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223053333A>G , CM000664.2:g.223053333A>G GRCh38
NC_000002.11:g.223918051A>G , CM000664.1:g.223918051A>G GRCh37
NC_000002.10:g.223626295A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000281830.4:c.503A>G MANE Select ENSP00000281830.5:p.Gln168Arg
ENST00000281830.3:c.656A>G ENSP00000281830.4:p.Gln219Arg
ENST00000488477.2:n.75+1059A>G
NM_080671.3:c.656A>G NP_542402.3:p.Gln219Arg
NM_080671.4:c.503A>G MANE Select NP_542402.4:p.Gln168Arg
Search 100 bp 5'
Search 100 bp 3'