Canonical Allele Identifier: CA393094063
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329754A>C , CM000677.2:g.73329754A>C GRCh38
NC_000015.9:g.73622095A>C , CM000677.1:g.73622095A>C GRCh37
NC_000015.8:g.71409148A>C NCBI36
NG_009063.1:g.44511T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1409T>G MANE Select ENSP00000261917.3:p.Phe470Cys
ENST00000261917.3:c.1409T>G ENSP00000261917.3:p.Phe470Cys
NM_005477.2:c.1409T>G NP_005468.1:p.Phe470Cys
XM_011521148.1:c.191T>G XP_011519450.1:p.Phe64Cys
XM_011521148.2:c.191T>G XP_011519450.1:p.Phe64Cys
NM_005477.3:c.1409T>G MANE Select NP_005468.1:p.Phe470Cys