Canonical Allele Identifier: CA2187186687
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322774G= , CM000677.2:g.73322774G= GRCh38
NC_000015.9:g.73615115G= , CM000677.1:g.73615115G= GRCh37
NC_000015.8:g.71402168G= NCBI36
NG_009063.1:g.51491C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3319C= MANE Select ENSP00000261917.3:p.His1107=
ENST00000261917.3:c.3319C= ENSP00000261917.3:p.His1107=
NM_005477.2:c.3319C= NP_005468.1:p.His1107=
XM_011521148.1:c.2101C= XP_011519450.1:p.His701=
XM_011521148.2:c.2101C= XP_011519450.1:p.His701=
NM_005477.3:c.3319C= MANE Select NP_005468.1:p.His1107=