Canonical Allele Identifier: CA393088480
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323442G>T , CM000677.2:g.73323442G>T GRCh38
NC_000015.9:g.73615783G>T , CM000677.1:g.73615783G>T GRCh37
NC_000015.8:g.71402836G>T NCBI36
NG_009063.1:g.50823C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2651C>A MANE Select ENSP00000261917.3:p.Pro884His
ENST00000261917.3:c.2651C>A ENSP00000261917.3:p.Pro884His
NM_005477.2:c.2651C>A NP_005468.1:p.Pro884His
XM_011521148.1:c.1433C>A XP_011519450.1:p.Pro478His
XM_011521148.2:c.1433C>A XP_011519450.1:p.Pro478His
NM_005477.3:c.2651C>A MANE Select NP_005468.1:p.Pro884His