Canonical Allele Identifier: CA7648824
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1731428
ClinVar RCV Id: RCV002457080 RCV003614103
dbSNP Id: rs549872016
ExAC: 15:73614996 G / A
gnomAD v2: 15-73614996-G-A
gnomAD v3: 15-73322655-G-A
gnomAD v4: 15-73322655-G-A
MyVariant Identifiers: chr15:g.73614996G>A (hg19) chr15:g.73322655G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322655G>A , CM000677.2:g.73322655G>A GRCh38
NC_000015.9:g.73614996G>A , CM000677.1:g.73614996G>A GRCh37
NC_000015.8:g.71402049G>A NCBI36
NG_009063.1:g.51610C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3438C>T MANE Select ENSP00000261917.3:p.Pro1146=
ENST00000261917.3:c.3438C>T ENSP00000261917.3:p.Pro1146=
NM_005477.2:c.3438C>T NP_005468.1:p.Pro1146=
XM_011521148.1:c.2220C>T XP_011519450.1:p.Pro740=
XM_011521148.2:c.2220C>T XP_011519450.1:p.Pro740=
NM_005477.3:c.3438C>T MANE Select NP_005468.1:p.Pro1146=
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Search 100 bp 3'