Canonical Allele Identifier: CA2187186455
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322687C= , CM000677.2:g.73322687C= GRCh38
NC_000015.9:g.73615028C= , CM000677.1:g.73615028C= GRCh37
NC_000015.8:g.71402081C= NCBI36
NG_009063.1:g.51578G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3406G= MANE Select ENSP00000261917.3:p.Gly1136=
ENST00000261917.3:c.3406G= ENSP00000261917.3:p.Gly1136=
NM_005477.2:c.3406G= NP_005468.1:p.Gly1136=
XM_011521148.1:c.2188G= XP_011519450.1:p.Gly730=
XM_011521148.2:c.2188G= XP_011519450.1:p.Gly730=
NM_005477.3:c.3406G= MANE Select NP_005468.1:p.Gly1136=