Canonical Allele Identifier: CA393097746
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011401
ClinVar RCV Id: RCV001309191
dbSNP Id: rs2043135514
gnomAD v4: 15-73367745-A-T
MyVariant Identifiers: chr15:g.73660086A>T (hg19) chr15:g.73367745A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367745A>T , CM000677.2:g.73367745A>T GRCh38
NC_000015.9:g.73660086A>T , CM000677.1:g.73660086A>T GRCh37
NC_000015.8:g.71447139A>T NCBI36
NG_009063.1:g.6520T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.526T>A MANE Select ENSP00000261917.3:p.Ser176Thr
ENST00000261917.3:c.526T>A ENSP00000261917.3:p.Ser176Thr
NM_005477.2:c.526T>A NP_005468.1:p.Ser176Thr
NM_005477.3:c.526T>A MANE Select NP_005468.1:p.Ser176Thr
Search 100 bp 5'
Search 100 bp 3'