Canonical Allele Identifier: CA2187167410
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329594G= , CM000677.2:g.73329594G= GRCh38
NC_000015.9:g.73621935G= , CM000677.1:g.73621935G= GRCh37
NC_000015.8:g.71408988G= NCBI36
NG_009063.1:g.44671C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1569C= MANE Select ENSP00000261917.3:p.Ser523=
ENST00000261917.3:c.1569C= ENSP00000261917.3:p.Ser523=
NM_005477.2:c.1569C= NP_005468.1:p.Ser523=
XM_011521148.1:c.351C= XP_011519450.1:p.Ser117=
XM_011521148.2:c.351C= XP_011519450.1:p.Ser117=
NM_005477.3:c.1569C= MANE Select NP_005468.1:p.Ser523=