Canonical Allele Identifier: CA393098687
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1787246
ClinVar RCV Id: RCV002432879
dbSNP Id: rs2043137805
gnomAD v3: 15-73368054-C-T
gnomAD v4: 15-73368054-C-T
MyVariant Identifiers: chr15:g.73660395C>T (hg19) chr15:g.73368054C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368054C>T , CM000677.2:g.73368054C>T GRCh38
NC_000015.9:g.73660395C>T , CM000677.1:g.73660395C>T GRCh37
NC_000015.8:g.71447448C>T NCBI36
NG_009063.1:g.6211G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.217G>A MANE Select ENSP00000261917.3:p.Gly73Arg
ENST00000261917.3:c.217G>A ENSP00000261917.3:p.Gly73Arg
NM_005477.2:c.217G>A NP_005468.1:p.Gly73Arg
NM_005477.3:c.217G>A MANE Select NP_005468.1:p.Gly73Arg
Search 100 bp 5'
Search 100 bp 3'