Canonical Allele Identifier: CA393085989
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322873G>T , CM000677.2:g.73322873G>T GRCh38
NC_000015.9:g.73615214G>T , CM000677.1:g.73615214G>T GRCh37
NC_000015.8:g.71402267G>T NCBI36
NG_009063.1:g.51392C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3220C>A MANE Select ENSP00000261917.3:p.Leu1074Ile
ENST00000261917.3:c.3220C>A ENSP00000261917.3:p.Leu1074Ile
NM_005477.2:c.3220C>A NP_005468.1:p.Leu1074Ile
XM_011521148.1:c.2002C>A XP_011519450.1:p.Leu668Ile
XM_011521148.2:c.2002C>A XP_011519450.1:p.Leu668Ile
NM_005477.3:c.3220C>A MANE Select NP_005468.1:p.Leu1074Ile