Canonical Allele Identifier: CA7649504
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 412789
dbSNP Id: rs764116333

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368169C>T , CM000677.2:g.73368169C>T GRCh38
NC_000015.9:g.73660510C>T , CM000677.1:g.73660510C>T GRCh37
NC_000015.8:g.71447563C>T NCBI36
NG_009063.1:g.6096G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.102G>A MANE Select ENSP00000261917.3:p.Glu34=
ENST00000261917.3:c.102G>A ENSP00000261917.3:p.Glu34=
NM_005477.2:c.102G>A NP_005468.1:p.Glu34=
NM_005477.3:c.102G>A MANE Select NP_005468.1:p.Glu34=