Canonical Allele Identifier: CA2187194510
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367704T= , CM000677.2:g.73367704T= GRCh38
NC_000015.9:g.73660045T= , CM000677.1:g.73660045T= GRCh37
NC_000015.8:g.71447098T= NCBI36
NG_009063.1:g.6561A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.567A= MANE Select ENSP00000261917.3:p.Lys189=
ENST00000261917.3:c.567A= ENSP00000261917.3:p.Lys189=
NM_005477.2:c.567A= NP_005468.1:p.Lys189=
NM_005477.3:c.567A= MANE Select NP_005468.1:p.Lys189=