Canonical Allele Identifier: CA393085052
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322580T>G , CM000677.2:g.73322580T>G GRCh38
NC_000015.9:g.73614921T>G , CM000677.1:g.73614921T>G GRCh37
NC_000015.8:g.71401974T>G NCBI36
NG_009063.1:g.51685A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3513A>C MANE Select ENSP00000261917.3:p.Arg1171Ser
ENST00000261917.3:c.3513A>C ENSP00000261917.3:p.Arg1171Ser
NM_005477.2:c.3513A>C NP_005468.1:p.Arg1171Ser
XM_011521148.1:c.2295A>C XP_011519450.1:p.Arg765Ser
XM_011521148.2:c.2295A>C XP_011519450.1:p.Arg765Ser
NM_005477.3:c.3513A>C MANE Select NP_005468.1:p.Arg1171Ser