Canonical Allele Identifier: CA393094065
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1409T>C MANE Select ENSP00000261917.3:p.Phe470Ser
ENST00000261917.3:c.1409T>C ENSP00000261917.3:p.Phe470Ser
NM_005477.2:c.1409T>C NP_005468.1:p.Phe470Ser
XM_011521148.1:c.191T>C XP_011519450.1:p.Phe64Ser
XM_011521148.2:c.191T>C XP_011519450.1:p.Phe64Ser
NM_005477.3:c.1409T>C MANE Select NP_005468.1:p.Phe470Ser