Canonical Allele Identifier: CA2629370507
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73322470-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322470A>G , CM000677.2:g.73322470A>G GRCh38
NC_000015.9:g.73614811A>G , CM000677.1:g.73614811A>G GRCh37
NC_000015.8:g.71401864A>G NCBI36
NG_009063.1:g.51795T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*11T>C MANE Select ENSP00000261917.3:n.*11T>C
ENST00000261917.3:c.*11T>C ENSP00000261917.3:n.*11T>C
NM_005477.2:c.*11T>C NP_005468.1:n.*11T>C
XM_011521148.1:c.*11T>C XP_011519450.1:n.*11T>C
XM_011521148.2:c.*11T>C XP_011519450.1:n.*11T>C
NM_005477.3:c.*11T>C MANE Select NP_005468.1:n.*11T>C
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