Canonical Allele Identifier: CA2187186274
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322580T= , CM000677.2:g.73322580T= GRCh38
NC_000015.9:g.73614921T= , CM000677.1:g.73614921T= GRCh37
NC_000015.8:g.71401974T= NCBI36
NG_009063.1:g.51685A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3513A= MANE Select ENSP00000261917.3:p.Arg1171=
ENST00000261917.3:c.3513A= ENSP00000261917.3:p.Arg1171=
NM_005477.2:c.3513A= NP_005468.1:p.Arg1171=
XM_011521148.1:c.2295A= XP_011519450.1:p.Arg765=
XM_011521148.2:c.2295A= XP_011519450.1:p.Arg765=
NM_005477.3:c.3513A= MANE Select NP_005468.1:p.Arg1171=