Canonical Allele Identifier: CA16614921
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 404133
dbSNP Id: rs1060500107

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329692C>T , CM000677.2:g.73329692C>T GRCh38
NC_000015.9:g.73622033C>T , CM000677.1:g.73622033C>T GRCh37
NC_000015.8:g.71409086C>T NCBI36
NG_009063.1:g.44573G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1471G>A MANE Select ENSP00000261917.3:p.Asp491Asn
ENST00000261917.3:c.1471G>A ENSP00000261917.3:p.Asp491Asn
NM_005477.2:c.1471G>A NP_005468.1:p.Asp491Asn
XM_011521148.1:c.253G>A XP_011519450.1:p.Asp85Asn
XM_011521148.2:c.253G>A XP_011519450.1:p.Asp85Asn
NM_005477.3:c.1471G>A MANE Select NP_005468.1:p.Asp491Asn