Canonical Allele Identifier: CA393086007
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322884C>G , CM000677.2:g.73322884C>G GRCh38
NC_000015.9:g.73615225C>G , CM000677.1:g.73615225C>G GRCh37
NC_000015.8:g.71402278C>G NCBI36
NG_009063.1:g.51381G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3209G>C MANE Select ENSP00000261917.3:p.Gly1070Ala
ENST00000261917.3:c.3209G>C ENSP00000261917.3:p.Gly1070Ala
NM_005477.2:c.3209G>C NP_005468.1:p.Gly1070Ala
XM_011521148.1:c.1991G>C XP_011519450.1:p.Gly664Ala
XM_011521148.2:c.1991G>C XP_011519450.1:p.Gly664Ala
NM_005477.3:c.3209G>C MANE Select NP_005468.1:p.Gly1070Ala