Canonical Allele Identifier: CA393097250
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2850631
ClinVar RCV Id: RCV003614714

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367590G>C , CM000677.2:g.73367590G>C GRCh38
NC_000015.9:g.73659931G>C , CM000677.1:g.73659931G>C GRCh37
NC_000015.8:g.71446984G>C NCBI36
NG_009063.1:g.6675C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.681C>G MANE Select ENSP00000261917.3:p.Asn227Lys
ENST00000261917.3:c.681C>G ENSP00000261917.3:p.Asn227Lys
NM_005477.2:c.681C>G NP_005468.1:p.Asn227Lys
NM_005477.3:c.681C>G MANE Select NP_005468.1:p.Asn227Lys