Canonical Allele Identifier: CA7649399
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2824559
ClinVar RCV Id: RCV003613833
dbSNP Id: rs563337210
ExAC: 15:73636032 C / T
gnomAD v2: 15-73636032-C-T
gnomAD v3: 15-73343691-C-T
gnomAD v4: 15-73343691-C-T
MyVariant Identifiers: chr15:g.73636032C>T (hg19) chr15:g.73343691C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343691C>T , CM000677.2:g.73343691C>T GRCh38
NC_000015.9:g.73636032C>T , CM000677.1:g.73636032C>T GRCh37
NC_000015.8:g.71423085C>T NCBI36
NG_009063.1:g.30574G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.903G>A MANE Select ENSP00000261917.3:p.Val301=
ENST00000261917.3:c.903G>A ENSP00000261917.3:p.Val301=
NM_005477.2:c.903G>A NP_005468.1:p.Val301=
NM_005477.3:c.903G>A MANE Select NP_005468.1:p.Val301=
Search 100 bp 5'
Search 100 bp 3'