Canonical Allele Identifier: CA2187188322
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323452A= , CM000677.2:g.73323452A= GRCh38
NC_000015.9:g.73615793A= , CM000677.1:g.73615793A= GRCh37
NC_000015.8:g.71402846A= NCBI36
NG_009063.1:g.50813T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2641T= MANE Select ENSP00000261917.3:p.Ser881=
ENST00000261917.3:c.2641T= ENSP00000261917.3:p.Ser881=
NM_005477.2:c.2641T= NP_005468.1:p.Ser881=
XM_011521148.1:c.1423T= XP_011519450.1:p.Ser475=
XM_011521148.2:c.1423T= XP_011519450.1:p.Ser475=
NM_005477.3:c.2641T= MANE Select NP_005468.1:p.Ser881=