Canonical Allele Identifier: CA393093967
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329731A>T , CM000677.2:g.73329731A>T GRCh38
NC_000015.9:g.73622072A>T , CM000677.1:g.73622072A>T GRCh37
NC_000015.8:g.71409125A>T NCBI36
NG_009063.1:g.44534T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1432T>A MANE Select ENSP00000261917.3:p.Cys478Ser
ENST00000261917.3:c.1432T>A ENSP00000261917.3:p.Cys478Ser
NM_005477.2:c.1432T>A NP_005468.1:p.Cys478Ser
XM_011521148.1:c.214T>A XP_011519450.1:p.Cys72Ser
XM_011521148.2:c.214T>A XP_011519450.1:p.Cys72Ser
NM_005477.3:c.1432T>A MANE Select NP_005468.1:p.Cys478Ser