Canonical Allele Identifier: CA247663
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 198825
ClinVar RCV Id: RCV000180279 RCV001210700 RCV002321709
dbSNP Id: rs750637152
ExAC: 15:73615303 C / T
gnomAD v2: 15-73615303-C-T
gnomAD v3: 15-73322962-C-T
gnomAD v4: 15-73322962-C-T
MyVariant Identifiers: chr15:g.73615303C>T (hg19) chr15:g.73322962C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322962C>T , CM000677.2:g.73322962C>T GRCh38
NC_000015.9:g.73615303C>T , CM000677.1:g.73615303C>T GRCh37
NC_000015.8:g.71402356C>T NCBI36
NG_009063.1:g.51303G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3131G>A MANE Select ENSP00000261917.3:p.Arg1044Gln
ENST00000261917.3:c.3131G>A ENSP00000261917.3:p.Arg1044Gln
NM_005477.2:c.3131G>A NP_005468.1:p.Arg1044Gln
XM_011521148.1:c.1913G>A XP_011519450.1:p.Arg638Gln
XM_011521148.2:c.1913G>A XP_011519450.1:p.Arg638Gln
NM_005477.3:c.3131G>A MANE Select NP_005468.1:p.Arg1044Gln
Search 100 bp 5'
Search 100 bp 3'