Canonical Allele Identifier: CA393098121
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423132
ClinVar RCV Id: RCV001926502 RCV002324341
dbSNP Id: rs1294780632
gnomAD v2: 15-73660206-C-T
gnomAD v4: 15-73367865-C-T
MyVariant Identifiers: chr15:g.73660206C>T (hg19) chr15:g.73367865C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367865C>T , CM000677.2:g.73367865C>T GRCh38
NC_000015.9:g.73660206C>T , CM000677.1:g.73660206C>T GRCh37
NC_000015.8:g.71447259C>T NCBI36
NG_009063.1:g.6400G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.406G>A MANE Select ENSP00000261917.3:p.Asp136Asn
ENST00000261917.3:c.406G>A ENSP00000261917.3:p.Asp136Asn
NM_005477.2:c.406G>A NP_005468.1:p.Asp136Asn
NM_005477.3:c.406G>A MANE Select NP_005468.1:p.Asp136Asn
Search 100 bp 5'
Search 100 bp 3'