Canonical Allele Identifier: CA491479597
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1654839
ClinVar RCV Id: RCV002156351
dbSNP Id: rs2151228505
gnomAD v4: 15-73367776-C-T
MyVariant Identifiers: chr15:g.73660117C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367776C>T , CM000677.2:g.73367776C>T GRCh38
NC_000015.9:g.73660117C>T , CM000677.1:g.73660117C>T GRCh37
NC_000015.8:g.71447170C>T NCBI36
NG_009063.1:g.6489G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.495G>A MANE Select ENSP00000261917.3:p.Pro165=
ENST00000261917.3:c.495G>A ENSP00000261917.3:p.Pro165=
NM_005477.2:c.495G>A NP_005468.1:p.Pro165=
NM_005477.3:c.495G>A MANE Select NP_005468.1:p.Pro165=
Search 100 bp 5'
Search 100 bp 3'