Canonical Allele Identifier: CA393093738
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329665T>A , CM000677.2:g.73329665T>A GRCh38
NC_000015.9:g.73622006T>A , CM000677.1:g.73622006T>A GRCh37
NC_000015.8:g.71409059T>A NCBI36
NG_009063.1:g.44600A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1498A>T MANE Select ENSP00000261917.3:p.Ile500Phe
ENST00000261917.3:c.1498A>T ENSP00000261917.3:p.Ile500Phe
NM_005477.2:c.1498A>T NP_005468.1:p.Ile500Phe
XM_011521148.1:c.280A>T XP_011519450.1:p.Ile94Phe
XM_011521148.2:c.280A>T XP_011519450.1:p.Ile94Phe
NM_005477.3:c.1498A>T MANE Select NP_005468.1:p.Ile500Phe