Canonical Allele Identifier: CA2187167590
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329713G= , CM000677.2:g.73329713G= GRCh38
NC_000015.9:g.73622054G= , CM000677.1:g.73622054G= GRCh37
NC_000015.8:g.71409107G= NCBI36
NG_009063.1:g.44552C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1450C= MANE Select ENSP00000261917.3:p.Gln484=
ENST00000261917.3:c.1450C= ENSP00000261917.3:p.Gln484=
NM_005477.2:c.1450C= NP_005468.1:p.Gln484=
XM_011521148.1:c.232C= XP_011519450.1:p.Gln78=
XM_011521148.2:c.232C= XP_011519450.1:p.Gln78=
NM_005477.3:c.1450C= MANE Select NP_005468.1:p.Gln484=