Canonical Allele Identifier: CA2187188320
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323450G= , CM000677.2:g.73323450G= GRCh38
NC_000015.9:g.73615791G= , CM000677.1:g.73615791G= GRCh37
NC_000015.8:g.71402844G= NCBI36
NG_009063.1:g.50815C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2643C= MANE Select ENSP00000261917.3:p.Ser881=
ENST00000261917.3:c.2643C= ENSP00000261917.3:p.Ser881=
NM_005477.2:c.2643C= NP_005468.1:p.Ser881=
XM_011521148.1:c.1425C= XP_011519450.1:p.Ser475=
XM_011521148.2:c.1425C= XP_011519450.1:p.Ser475=
NM_005477.3:c.2643C= MANE Select NP_005468.1:p.Ser881=