Canonical Allele Identifier: CA7648999
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1433354
ClinVar RCV Id: RCV001982227
dbSNP Id: rs779963031
ExAC: 15:73615871 A / G
gnomAD v2: 15-73615871-A-G
gnomAD v3: 15-73323530-A-G
gnomAD v4: 15-73323530-A-G
MyVariant Identifiers: chr15:g.73615871A>G (hg19) chr15:g.73323530A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323530A>G , CM000677.2:g.73323530A>G GRCh38
NC_000015.9:g.73615871A>G , CM000677.1:g.73615871A>G GRCh37
NC_000015.8:g.71402924A>G NCBI36
NG_009063.1:g.50735T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2563T>C MANE Select ENSP00000261917.3:p.Ser855Pro
ENST00000261917.3:c.2563T>C ENSP00000261917.3:p.Ser855Pro
NM_005477.2:c.2563T>C NP_005468.1:p.Ser855Pro
XM_011521148.1:c.1345T>C XP_011519450.1:p.Ser449Pro
XM_011521148.2:c.1345T>C XP_011519450.1:p.Ser449Pro
NM_005477.3:c.2563T>C MANE Select NP_005468.1:p.Ser855Pro
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