Canonical Allele Identifier: CA2187194696
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368069G= , CM000677.2:g.73368069G= GRCh38
NC_000015.9:g.73660410G= , CM000677.1:g.73660410G= GRCh37
NC_000015.8:g.71447463G= NCBI36
NG_009063.1:g.6196C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.202C= MANE Select ENSP00000261917.3:p.Arg68=
ENST00000261917.3:c.202C= ENSP00000261917.3:p.Arg68=
NM_005477.2:c.202C= NP_005468.1:p.Arg68=
NM_005477.3:c.202C= MANE Select NP_005468.1:p.Arg68=