Canonical Allele Identifier: CA431669533
Gene: KCNE4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.223917890C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223053172C>G , CM000664.2:g.223053172C>G GRCh38
NC_000002.11:g.223917890C>G , CM000664.1:g.223917890C>G GRCh37
NC_000002.10:g.223626134C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000281830.4:c.342C>G MANE Select ENSP00000281830.5:p.Ser114=
ENST00000281830.3:c.495C>G ENSP00000281830.4:p.Ser165=
ENST00000488477.2:n.75+898C>G
NM_080671.3:c.495C>G NP_542402.3:p.Ser165=
NM_080671.4:c.342C>G MANE Select NP_542402.4:p.Ser114=
Search 100 bp 5'
Search 100 bp 3'