Canonical Allele Identifier: CA393093780
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1363278
ClinVar RCV Id: RCV001902170 RCV002223318
dbSNP Id: rs2151217007
gnomAD v4: 15-73329683-G-A
MyVariant Identifiers: chr15:g.73622024G>A (hg19) chr15:g.73329683G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329683G>A , CM000677.2:g.73329683G>A GRCh38
NC_000015.9:g.73622024G>A , CM000677.1:g.73622024G>A GRCh37
NC_000015.8:g.71409077G>A NCBI36
NG_009063.1:g.44582C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1480C>T MANE Select ENSP00000261917.3:p.Leu494Phe
ENST00000261917.3:c.1480C>T ENSP00000261917.3:p.Leu494Phe
NM_005477.2:c.1480C>T NP_005468.1:p.Leu494Phe
XM_011521148.1:c.262C>T XP_011519450.1:p.Leu88Phe
XM_011521148.2:c.262C>T XP_011519450.1:p.Leu88Phe
NM_005477.3:c.1480C>T MANE Select NP_005468.1:p.Leu494Phe
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