Canonical Allele Identifier: CA393097450
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1505528
ClinVar RCV Id: RCV002004104
dbSNP Id: rs2151228416
MyVariant Identifiers: chr15:g.73659993G>A (hg19) chr15:g.73367652G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367652G>A , CM000677.2:g.73367652G>A GRCh38
NC_000015.9:g.73659993G>A , CM000677.1:g.73659993G>A GRCh37
NC_000015.8:g.71447046G>A NCBI36
NG_009063.1:g.6613C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.619C>T MANE Select ENSP00000261917.3:p.Arg207Cys
ENST00000261917.3:c.619C>T ENSP00000261917.3:p.Arg207Cys
NM_005477.2:c.619C>T NP_005468.1:p.Arg207Cys
NM_005477.3:c.619C>T MANE Select NP_005468.1:p.Arg207Cys
Search 100 bp 5'
Search 100 bp 3'