Canonical Allele Identifier: CA393086651
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323128C>G , CM000677.2:g.73323128C>G GRCh38
NC_000015.9:g.73615469C>G , CM000677.1:g.73615469C>G GRCh37
NC_000015.8:g.71402522C>G NCBI36
NG_009063.1:g.51137G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2965G>C MANE Select ENSP00000261917.3:p.Gly989Arg
ENST00000261917.3:c.2965G>C ENSP00000261917.3:p.Gly989Arg
NM_005477.2:c.2965G>C NP_005468.1:p.Gly989Arg
XM_011521148.1:c.1747G>C XP_011519450.1:p.Gly583Arg
XM_011521148.2:c.1747G>C XP_011519450.1:p.Gly583Arg
NM_005477.3:c.2965G>C MANE Select NP_005468.1:p.Gly989Arg