Canonical Allele Identifier: CA393098532
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2265118
ClinVar RCV Id: RCV004118635
gnomAD v4: 15-73368001-G-T
MyVariant Identifiers: chr15:g.73660342G>T (hg19) chr15:g.73368001G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368001G>T , CM000677.2:g.73368001G>T GRCh38
NC_000015.9:g.73660342G>T , CM000677.1:g.73660342G>T GRCh37
NC_000015.8:g.71447395G>T NCBI36
NG_009063.1:g.6264C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.270C>A MANE Select ENSP00000261917.3:p.Asn90Lys
ENST00000261917.3:c.270C>A ENSP00000261917.3:p.Asn90Lys
NM_005477.2:c.270C>A NP_005468.1:p.Asn90Lys
NM_005477.3:c.270C>A MANE Select NP_005468.1:p.Asn90Lys
Search 100 bp 5'
Search 100 bp 3'