Canonical Allele Identifier: CA393085047
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322579C>G , CM000677.2:g.73322579C>G GRCh38
NC_000015.9:g.73614920C>G , CM000677.1:g.73614920C>G GRCh37
NC_000015.8:g.71401973C>G NCBI36
NG_009063.1:g.51686G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3514G>C MANE Select ENSP00000261917.3:p.Ala1172Pro
ENST00000261917.3:c.3514G>C ENSP00000261917.3:p.Ala1172Pro
NM_005477.2:c.3514G>C NP_005468.1:p.Ala1172Pro
XM_011521148.1:c.2296G>C XP_011519450.1:p.Ala766Pro
XM_011521148.2:c.2296G>C XP_011519450.1:p.Ala766Pro
NM_005477.3:c.3514G>C MANE Select NP_005468.1:p.Ala1172Pro