Canonical Allele Identifier: CA393089009
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323715A>G , CM000677.2:g.73323715A>G GRCh38
NC_000015.9:g.73616056A>G , CM000677.1:g.73616056A>G GRCh37
NC_000015.8:g.71403109A>G NCBI36
NG_009063.1:g.50550T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2378T>C MANE Select ENSP00000261917.3:p.Ile793Thr
ENST00000261917.3:c.2378T>C ENSP00000261917.3:p.Ile793Thr
NM_005477.2:c.2378T>C NP_005468.1:p.Ile793Thr
XM_011521148.1:c.1160T>C XP_011519450.1:p.Ile387Thr
XM_011521148.2:c.1160T>C XP_011519450.1:p.Ile387Thr
NM_005477.3:c.2378T>C MANE Select NP_005468.1:p.Ile793Thr