Canonical Allele Identifier: CA393095262
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058283
ClinVar RCV Id: RCV001367402 RCV002377540
dbSNP Id: rs1272107414
gnomAD v2: 15-73636020-G-T
gnomAD v3: 15-73343679-G-T
gnomAD v4: 15-73343679-G-T
MyVariant Identifiers: chr15:g.73636020G>T (hg19) chr15:g.73343679G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343679G>T , CM000677.2:g.73343679G>T GRCh38
NC_000015.9:g.73636020G>T , CM000677.1:g.73636020G>T GRCh37
NC_000015.8:g.71423073G>T NCBI36
NG_009063.1:g.30586C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.915C>A MANE Select ENSP00000261917.3:p.Phe305Leu
ENST00000261917.3:c.915C>A ENSP00000261917.3:p.Phe305Leu
NM_005477.2:c.915C>A NP_005468.1:p.Phe305Leu
NM_005477.3:c.915C>A MANE Select NP_005468.1:p.Phe305Leu
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