Canonical Allele Identifier: CA765344109
Gene: KCNE4 HGNC NCBI

Linked Data

dbSNP Id: rs1177071417
gnomAD v3: 2-223053640-A-G
gnomAD v4: 2-223053640-A-G
MyVariant Identifiers: chr2:g.223918358A>G (hg19) chr2:g.223053640A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223053640A>G , CM000664.2:g.223053640A>G GRCh38
NC_000002.11:g.223918358A>G , CM000664.1:g.223918358A>G GRCh37
NC_000002.10:g.223626602A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000281830.4:c.*297A>G MANE Select ENSP00000281830.5:n.*297A>G
ENST00000281830.3:c.*297A>G ENSP00000281830.4:n.*297A>G
ENST00000488477.2:n.75+1366A>G
NM_080671.3:c.*297A>G NP_542402.3:n.*297A>G
NM_080671.4:c.*297A>G MANE Select NP_542402.4:n.*297A>G
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