Canonical Allele Identifier: CA7648848
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730087
ClinVar RCV Id: RCV002326315
dbSNP Id: rs771606277
ExAC: 15:73615124 C / T
gnomAD v2: 15-73615124-C-T
gnomAD v4: 15-73322783-C-T
MyVariant Identifiers: chr15:g.73615124C>T (hg19) chr15:g.73322783C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322783C>T , CM000677.2:g.73322783C>T GRCh38
NC_000015.9:g.73615124C>T , CM000677.1:g.73615124C>T GRCh37
NC_000015.8:g.71402177C>T NCBI36
NG_009063.1:g.51482G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3310G>A MANE Select ENSP00000261917.3:p.Ala1104Thr
ENST00000261917.3:c.3310G>A ENSP00000261917.3:p.Ala1104Thr
NM_005477.2:c.3310G>A NP_005468.1:p.Ala1104Thr
XM_011521148.1:c.2092G>A XP_011519450.1:p.Ala698Thr
XM_011521148.2:c.2092G>A XP_011519450.1:p.Ala698Thr
NM_005477.3:c.3310G>A MANE Select NP_005468.1:p.Ala1104Thr
Search 100 bp 5'
Search 100 bp 3'