Canonical Allele Identifier: CA2187194517
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367715T= , CM000677.2:g.73367715T= GRCh38
NC_000015.9:g.73660056T= , CM000677.1:g.73660056T= GRCh37
NC_000015.8:g.71447109T= NCBI36
NG_009063.1:g.6550A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.556A= MANE Select ENSP00000261917.3:p.Thr186=
ENST00000261917.3:c.556A= ENSP00000261917.3:p.Thr186=
NM_005477.2:c.556A= NP_005468.1:p.Thr186=
NM_005477.3:c.556A= MANE Select NP_005468.1:p.Thr186=