Canonical Allele Identifier: CA393086011
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs760242560

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322887C>G , CM000677.2:g.73322887C>G GRCh38
NC_000015.9:g.73615228C>G , CM000677.1:g.73615228C>G GRCh37
NC_000015.8:g.71402281C>G NCBI36
NG_009063.1:g.51378G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3206G>C MANE Select ENSP00000261917.3:p.Arg1069Pro
ENST00000261917.3:c.3206G>C ENSP00000261917.3:p.Arg1069Pro
NM_005477.2:c.3206G>C NP_005468.1:p.Arg1069Pro
XM_011521148.1:c.1988G>C XP_011519450.1:p.Arg663Pro
XM_011521148.2:c.1988G>C XP_011519450.1:p.Arg663Pro
NM_005477.3:c.3206G>C MANE Select NP_005468.1:p.Arg1069Pro