Canonical Allele Identifier: CA393085391
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs761421530

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322687C>G , CM000677.2:g.73322687C>G GRCh38
NC_000015.9:g.73615028C>G , CM000677.1:g.73615028C>G GRCh37
NC_000015.8:g.71402081C>G NCBI36
NG_009063.1:g.51578G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3406G>C MANE Select ENSP00000261917.3:p.Gly1136Arg
ENST00000261917.3:c.3406G>C ENSP00000261917.3:p.Gly1136Arg
NM_005477.2:c.3406G>C NP_005468.1:p.Gly1136Arg
XM_011521148.1:c.2188G>C XP_011519450.1:p.Gly730Arg
XM_011521148.2:c.2188G>C XP_011519450.1:p.Gly730Arg
NM_005477.3:c.3406G>C MANE Select NP_005468.1:p.Gly1136Arg