Canonical Allele Identifier: CA7648890
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 470663
ClinVar RCV Id: RCV000559988 RCV002506357 RCV004538033 RCV002223873
dbSNP Id: rs762950777
ExAC: 15:73615370 G / A
gnomAD v2: 15-73615370-G-A
gnomAD v3: 15-73323029-G-A
gnomAD v4: 15-73323029-G-A
MyVariant Identifiers: chr15:g.73615370G>A (hg19) chr15:g.73323029G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323029G>A , CM000677.2:g.73323029G>A GRCh38
NC_000015.9:g.73615370G>A , CM000677.1:g.73615370G>A GRCh37
NC_000015.8:g.71402423G>A NCBI36
NG_009063.1:g.51236C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3064C>T MANE Select ENSP00000261917.3:p.Arg1022Ter
ENST00000261917.3:c.3064C>T ENSP00000261917.3:p.Arg1022Ter
NM_005477.2:c.3064C>T NP_005468.1:p.Arg1022Ter
XM_011521148.1:c.1846C>T XP_011519450.1:p.Arg616Ter
XM_011521148.2:c.1846C>T XP_011519450.1:p.Arg616Ter
NM_005477.3:c.3064C>T MANE Select NP_005468.1:p.Arg1022Ter
Search 100 bp 5'
Search 100 bp 3'