Canonical Allele Identifier: CA393097737
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367742C>T , CM000677.2:g.73367742C>T GRCh38
NC_000015.9:g.73660083C>T , CM000677.1:g.73660083C>T GRCh37
NC_000015.8:g.71447136C>T NCBI36
NG_009063.1:g.6523G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.529G>A MANE Select ENSP00000261917.3:p.Ala177Thr
ENST00000261917.3:c.529G>A ENSP00000261917.3:p.Ala177Thr
NM_005477.2:c.529G>A NP_005468.1:p.Ala177Thr
NM_005477.3:c.529G>A MANE Select NP_005468.1:p.Ala177Thr