Canonical Allele Identifier: CA393093686
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 646340
ClinVar RCV Id: RCV000800610
dbSNP Id: rs1595822914
MyVariant Identifiers: chr15:g.73621993G>T (hg19) chr15:g.73329652G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329652G>T , CM000677.2:g.73329652G>T GRCh38
NC_000015.9:g.73621993G>T , CM000677.1:g.73621993G>T GRCh37
NC_000015.8:g.71409046G>T NCBI36
NG_009063.1:g.44613C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1511C>A MANE Select ENSP00000261917.3:p.Thr504Asn
ENST00000261917.3:c.1511C>A ENSP00000261917.3:p.Thr504Asn
NM_005477.2:c.1511C>A NP_005468.1:p.Thr504Asn
XM_011521148.1:c.293C>A XP_011519450.1:p.Thr98Asn
XM_011521148.2:c.293C>A XP_011519450.1:p.Thr98Asn
NM_005477.3:c.1511C>A MANE Select NP_005468.1:p.Thr504Asn
Search 100 bp 5'
Search 100 bp 3'