Canonical Allele Identifier: CA2187167375
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329575T= , CM000677.2:g.73329575T= GRCh38
NC_000015.9:g.73621916T= , CM000677.1:g.73621916T= GRCh37
NC_000015.8:g.71408969T= NCBI36
NG_009063.1:g.44690A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1588A= MANE Select ENSP00000261917.3:p.Lys530=
ENST00000261917.3:c.1588A= ENSP00000261917.3:p.Lys530=
NM_005477.2:c.1588A= NP_005468.1:p.Lys530=
XM_011521148.1:c.370A= XP_011519450.1:p.Lys124=
XM_011521148.2:c.370A= XP_011519450.1:p.Lys124=
NM_005477.3:c.1588A= MANE Select NP_005468.1:p.Lys530=