Canonical Allele Identifier: CA491479554
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1607623
ClinVar RCV Id: RCV002144715
dbSNP Id: rs2151228455
MyVariant Identifiers: chr15:g.73660054G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367713G>C , CM000677.2:g.73367713G>C GRCh38
NC_000015.9:g.73660054G>C , CM000677.1:g.73660054G>C GRCh37
NC_000015.8:g.71447107G>C NCBI36
NG_009063.1:g.6552C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.558C>G MANE Select ENSP00000261917.3:p.Thr186=
ENST00000261917.3:c.558C>G ENSP00000261917.3:p.Thr186=
NM_005477.2:c.558C>G NP_005468.1:p.Thr186=
NM_005477.3:c.558C>G MANE Select NP_005468.1:p.Thr186=
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