Canonical Allele Identifier: CA351121631
Gene: KCNE4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.223918022C>A (hg19) chr2:g.223053304C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223053304C>A , CM000664.2:g.223053304C>A GRCh38
NC_000002.11:g.223918022C>A , CM000664.1:g.223918022C>A GRCh37
NC_000002.10:g.223626266C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000281830.4:c.474C>A MANE Select ENSP00000281830.5:p.Ser158Arg
ENST00000281830.3:c.627C>A ENSP00000281830.4:p.Ser209Arg
ENST00000488477.2:n.75+1030C>A
NM_080671.3:c.627C>A NP_542402.3:p.Ser209Arg
NM_080671.4:c.474C>A MANE Select NP_542402.4:p.Ser158Arg
Search 100 bp 5'
Search 100 bp 3'