Canonical Allele Identifier: CA393093807
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329695A>C , CM000677.2:g.73329695A>C GRCh38
NC_000015.9:g.73622036A>C , CM000677.1:g.73622036A>C GRCh37
NC_000015.8:g.71409089A>C NCBI36
NG_009063.1:g.44570T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1468T>G MANE Select ENSP00000261917.3:p.Ser490Ala
ENST00000261917.3:c.1468T>G ENSP00000261917.3:p.Ser490Ala
NM_005477.2:c.1468T>G NP_005468.1:p.Ser490Ala
XM_011521148.1:c.250T>G XP_011519450.1:p.Ser84Ala
XM_011521148.2:c.250T>G XP_011519450.1:p.Ser84Ala
NM_005477.3:c.1468T>G MANE Select NP_005468.1:p.Ser490Ala