Canonical Allele Identifier: CA2804726804
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322412T>G , CM000677.2:g.73322412T>G GRCh38
NC_000015.9:g.73614753T>G , CM000677.1:g.73614753T>G GRCh37
NC_000015.8:g.71401806T>G NCBI36
NG_009063.1:g.51853A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*69A>C MANE Select ENSP00000261917.3:n.*69A>C
ENST00000261917.3:c.*69A>C ENSP00000261917.3:n.*69A>C
NM_005477.2:c.*69A>C NP_005468.1:n.*69A>C
XM_011521148.1:c.*69A>C XP_011519450.1:n.*69A>C
XM_011521148.2:c.*69A>C XP_011519450.1:n.*69A>C
NM_005477.3:c.*69A>C MANE Select NP_005468.1:n.*69A>C
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