Canonical Allele Identifier: CA393097677
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367724A>T , CM000677.2:g.73367724A>T GRCh38
NC_000015.9:g.73660065A>T , CM000677.1:g.73660065A>T GRCh37
NC_000015.8:g.71447118A>T NCBI36
NG_009063.1:g.6541T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.547T>A MANE Select ENSP00000261917.3:p.Ser183Thr
ENST00000261917.3:c.547T>A ENSP00000261917.3:p.Ser183Thr
NM_005477.2:c.547T>A NP_005468.1:p.Ser183Thr
NM_005477.3:c.547T>A MANE Select NP_005468.1:p.Ser183Thr