Canonical Allele Identifier: CA2187194654
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367989C= , CM000677.2:g.73367989C= GRCh38
NC_000015.9:g.73660330C= , CM000677.1:g.73660330C= GRCh37
NC_000015.8:g.71447383C= NCBI36
NG_009063.1:g.6276G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.282G= MANE Select ENSP00000261917.3:p.Arg94=
ENST00000261917.3:c.282G= ENSP00000261917.3:p.Arg94=
NM_005477.2:c.282G= NP_005468.1:p.Arg94=
NM_005477.3:c.282G= MANE Select NP_005468.1:p.Arg94=