Canonical Allele Identifier: CA393097953
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741871
ClinVar RCV Id: RCV002342438
gnomAD v4: 15-73367811-G-A
MyVariant Identifiers: chr15:g.73660152G>A (hg19) chr15:g.73367811G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367811G>A , CM000677.2:g.73367811G>A GRCh38
NC_000015.9:g.73660152G>A , CM000677.1:g.73660152G>A GRCh37
NC_000015.8:g.71447205G>A NCBI36
NG_009063.1:g.6454C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.460C>T MANE Select ENSP00000261917.3:p.Arg154Cys
ENST00000261917.3:c.460C>T ENSP00000261917.3:p.Arg154Cys
NM_005477.2:c.460C>T NP_005468.1:p.Arg154Cys
NM_005477.3:c.460C>T MANE Select NP_005468.1:p.Arg154Cys
Search 100 bp 5'
Search 100 bp 3'