Canonical Allele Identifier: CA393086130
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042871271

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322948G>C , CM000677.2:g.73322948G>C GRCh38
NC_000015.9:g.73615289G>C , CM000677.1:g.73615289G>C GRCh37
NC_000015.8:g.71402342G>C NCBI36
NG_009063.1:g.51317C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3145C>G MANE Select ENSP00000261917.3:p.His1049Asp
ENST00000261917.3:c.3145C>G ENSP00000261917.3:p.His1049Asp
NM_005477.2:c.3145C>G NP_005468.1:p.His1049Asp
XM_011521148.1:c.1927C>G XP_011519450.1:p.His643Asp
XM_011521148.2:c.1927C>G XP_011519450.1:p.His643Asp
NM_005477.3:c.3145C>G MANE Select NP_005468.1:p.His1049Asp