Canonical Allele Identifier: CA222867
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 95283
dbSNP Id: rs200303699

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332122C>T , CM000677.2:g.73332122C>T GRCh38
NC_000015.9:g.73624463C>T , CM000677.1:g.73624463C>T GRCh37
NC_000015.8:g.71411516C>T NCBI36
NG_009063.1:g.42143G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1371+9G>A MANE Select ENSP00000261917.3:p.=
ENST00000261917.3:c.1371+9G>A ENSP00000261917.3:p.=
NM_005477.2:c.1371+9G>A NP_005468.1:p.=
XM_011521148.1:c.153+9G>A XP_011519450.1:p.=
XM_011521148.2:c.153+9G>A XP_011519450.1:p.=
NM_005477.3:c.1371+9G>A MANE Select NP_005468.1:p.=