Canonical Allele Identifier: CA7649052
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789357
ClinVar RCV Id: RCV002446381
dbSNP Id: rs764093328
ExAC: 15:73616128 G / T
gnomAD v2: 15-73616128-G-T
gnomAD v4: 15-73323787-G-T
MyVariant Identifiers: chr15:g.73616128G>T (hg19) chr15:g.73323787G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323787G>T , CM000677.2:g.73323787G>T GRCh38
NC_000015.9:g.73616128G>T , CM000677.1:g.73616128G>T GRCh37
NC_000015.8:g.71403181G>T NCBI36
NG_009063.1:g.50478C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2306C>A MANE Select ENSP00000261917.3:p.Pro769His
ENST00000261917.3:c.2306C>A ENSP00000261917.3:p.Pro769His
NM_005477.2:c.2306C>A NP_005468.1:p.Pro769His
XM_011521148.1:c.1088C>A XP_011519450.1:p.Pro363His
XM_011521148.2:c.1088C>A XP_011519450.1:p.Pro363His
NM_005477.3:c.2306C>A MANE Select NP_005468.1:p.Pro769His
Search 100 bp 5'
Search 100 bp 3'