Canonical Allele Identifier: CA393085347
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322665C>T , CM000677.2:g.73322665C>T GRCh38
NC_000015.9:g.73615006C>T , CM000677.1:g.73615006C>T GRCh37
NC_000015.8:g.71402059C>T NCBI36
NG_009063.1:g.51600G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3428G>A MANE Select ENSP00000261917.3:p.Gly1143Asp
ENST00000261917.3:c.3428G>A ENSP00000261917.3:p.Gly1143Asp
NM_005477.2:c.3428G>A NP_005468.1:p.Gly1143Asp
XM_011521148.1:c.2210G>A XP_011519450.1:p.Gly737Asp
XM_011521148.2:c.2210G>A XP_011519450.1:p.Gly737Asp
NM_005477.3:c.3428G>A MANE Select NP_005468.1:p.Gly1143Asp