Canonical Allele Identifier: CA393093424
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329598G>C , CM000677.2:g.73329598G>C GRCh38
NC_000015.9:g.73621939G>C , CM000677.1:g.73621939G>C GRCh37
NC_000015.8:g.71408992G>C NCBI36
NG_009063.1:g.44667C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1565C>G MANE Select ENSP00000261917.3:p.Ser522Cys
ENST00000261917.3:c.1565C>G ENSP00000261917.3:p.Ser522Cys
NM_005477.2:c.1565C>G NP_005468.1:p.Ser522Cys
XM_011521148.1:c.347C>G XP_011519450.1:p.Ser116Cys
XM_011521148.2:c.347C>G XP_011519450.1:p.Ser116Cys
NM_005477.3:c.1565C>G MANE Select NP_005468.1:p.Ser522Cys