Canonical Allele Identifier: CA7648875
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728502
ClinVar RCV Id: RCV002322705 RCV003099265
dbSNP Id: rs764262532
ExAC: 15:73615255 G / T
gnomAD v2: 15-73615255-G-T
gnomAD v3: 15-73322914-G-T
gnomAD v4: 15-73322914-G-T
MyVariant Identifiers: chr15:g.73615255G>T (hg19) chr15:g.73322914G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322914G>T , CM000677.2:g.73322914G>T GRCh38
NC_000015.9:g.73615255G>T , CM000677.1:g.73615255G>T GRCh37
NC_000015.8:g.71402308G>T NCBI36
NG_009063.1:g.51351C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3179C>A MANE Select ENSP00000261917.3:p.Pro1060His
ENST00000261917.3:c.3179C>A ENSP00000261917.3:p.Pro1060His
NM_005477.2:c.3179C>A NP_005468.1:p.Pro1060His
XM_011521148.1:c.1961C>A XP_011519450.1:p.Pro654His
XM_011521148.2:c.1961C>A XP_011519450.1:p.Pro654His
NM_005477.3:c.3179C>A MANE Select NP_005468.1:p.Pro1060His
Search 100 bp 5'
Search 100 bp 3'