Canonical Allele Identifier: CA7648815
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 849884
ClinVar RCV Id: RCV001053934
dbSNP Id: rs750255859
ExAC: 15:73614944 G / C
gnomAD v2: 15-73614944-G-C
gnomAD v3: 15-73322603-G-C
gnomAD v4: 15-73322603-G-C
MyVariant Identifiers: chr15:g.73614944G>C (hg19) chr15:g.73322603G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322603G>C , CM000677.2:g.73322603G>C GRCh38
NC_000015.9:g.73614944G>C , CM000677.1:g.73614944G>C GRCh37
NC_000015.8:g.71401997G>C NCBI36
NG_009063.1:g.51662C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3490C>G MANE Select ENSP00000261917.3:p.Pro1164Ala
ENST00000261917.3:c.3490C>G ENSP00000261917.3:p.Pro1164Ala
NM_005477.2:c.3490C>G NP_005468.1:p.Pro1164Ala
XM_011521148.1:c.2272C>G XP_011519450.1:p.Pro758Ala
XM_011521148.2:c.2272C>G XP_011519450.1:p.Pro758Ala
NM_005477.3:c.3490C>G MANE Select NP_005468.1:p.Pro1164Ala
Search 100 bp 5'
Search 100 bp 3'