Canonical Allele Identifier: CA393085169
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322614G>C , CM000677.2:g.73322614G>C GRCh38
NC_000015.9:g.73614955G>C , CM000677.1:g.73614955G>C GRCh37
NC_000015.8:g.71402008G>C NCBI36
NG_009063.1:g.51651C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3479C>G MANE Select ENSP00000261917.3:p.Ser1160Cys
ENST00000261917.3:c.3479C>G ENSP00000261917.3:p.Ser1160Cys
NM_005477.2:c.3479C>G NP_005468.1:p.Ser1160Cys
XM_011521148.1:c.2261C>G XP_011519450.1:p.Ser754Cys
XM_011521148.2:c.2261C>G XP_011519450.1:p.Ser754Cys
NM_005477.3:c.3479C>G MANE Select NP_005468.1:p.Ser1160Cys