Canonical Allele Identifier: CA7648871
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 663635
ClinVar RCV Id: RCV000821551 RCV002487844
dbSNP Id: rs776270218
ExAC: 15:73615231 C / T
gnomAD v2: 15-73615231-C-T
gnomAD v3: 15-73322890-C-T
gnomAD v4: 15-73322890-C-T
MyVariant Identifiers: chr15:g.73615231C>T (hg19) chr15:g.73322890C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322890C>T , CM000677.2:g.73322890C>T GRCh38
NC_000015.9:g.73615231C>T , CM000677.1:g.73615231C>T GRCh37
NC_000015.8:g.71402284C>T NCBI36
NG_009063.1:g.51375G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3203G>A MANE Select ENSP00000261917.3:p.Arg1068His
ENST00000261917.3:c.3203G>A ENSP00000261917.3:p.Arg1068His
NM_005477.2:c.3203G>A NP_005468.1:p.Arg1068His
XM_011521148.1:c.1985G>A XP_011519450.1:p.Arg662His
XM_011521148.2:c.1985G>A XP_011519450.1:p.Arg662His
NM_005477.3:c.3203G>A MANE Select NP_005468.1:p.Arg1068His
Search 100 bp 5'
Search 100 bp 3'