Canonical Allele Identifier: CA238824
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 180370
ClinVar RCV Id: RCV000157245 RCV000618430 RCV000723946 RCV000852712 RCV001082507 RCV001117433
dbSNP Id: rs560874115
ExAC: 15:73660154 T / C
gnomAD v2: 15-73660154-T-C
gnomAD v3: 15-73367813-T-C
gnomAD v4: 15-73367813-T-C
MyVariant Identifiers: chr15:g.73660154T>C (hg19) chr15:g.73367813T>C (hg38)
PubMed: PMID:24607718 PMID:28254188 PMID:28341588
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367813T>C , CM000677.2:g.73367813T>C GRCh38
NC_000015.9:g.73660154T>C , CM000677.1:g.73660154T>C GRCh37
NC_000015.8:g.71447207T>C NCBI36
NG_009063.1:g.6452A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.458A>G MANE Select ENSP00000261917.3:p.Glu153Gly
ENST00000261917.3:c.458A>G ENSP00000261917.3:p.Glu153Gly
NM_005477.2:c.458A>G NP_005468.1:p.Glu153Gly
NM_005477.3:c.458A>G MANE Select NP_005468.1:p.Glu153Gly
Search 100 bp 5'
Search 100 bp 3'