Canonical Allele Identifier: CA2187194699
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368075C= , CM000677.2:g.73368075C= GRCh38
NC_000015.9:g.73660416C= , CM000677.1:g.73660416C= GRCh37
NC_000015.8:g.71447469C= NCBI36
NG_009063.1:g.6190G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.196G= MANE Select ENSP00000261917.3:p.Glu66=
ENST00000261917.3:c.196G= ENSP00000261917.3:p.Glu66=
NM_005477.2:c.196G= NP_005468.1:p.Glu66=
NM_005477.3:c.196G= MANE Select NP_005468.1:p.Glu66=