Canonical Allele Identifier: CA393097373
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302069
ClinVar RCV Id: RCV001753958 RCV003382634
dbSNP Id: rs2151228399
gnomAD v4: 15-73367627-T-C
MyVariant Identifiers: chr15:g.73659968T>C (hg19) chr15:g.73367627T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367627T>C , CM000677.2:g.73367627T>C GRCh38
NC_000015.9:g.73659968T>C , CM000677.1:g.73659968T>C GRCh37
NC_000015.8:g.71447021T>C NCBI36
NG_009063.1:g.6638A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.644A>G MANE Select ENSP00000261917.3:p.Gln215Arg
ENST00000261917.3:c.644A>G ENSP00000261917.3:p.Gln215Arg
NM_005477.2:c.644A>G NP_005468.1:p.Gln215Arg
NM_005477.3:c.644A>G MANE Select NP_005468.1:p.Gln215Arg
Search 100 bp 5'
Search 100 bp 3'