Canonical Allele Identifier: CA2629389853
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73367945-CCG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367947_73367948del , CM000677.2:g.73367947_73367948del GRCh38
NC_000015.9:g.73660288_73660289del , CM000677.1:g.73660288_73660289del GRCh37
NC_000015.8:g.71447341_71447342del NCBI36
NG_009063.1:g.6318_6319del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.324_325del MANE Select ENSP00000261917.3:p.Gly109GlnfsTer15
ENST00000261917.3:c.324_325del ENSP00000261917.3:p.Gly109GlnfsTer15
NM_005477.2:c.324_325del NP_005468.1:p.Gly109GlnfsTer15
NM_005477.3:c.324_325del MANE Select NP_005468.1:p.Gly109GlnfsTer15
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Search 100 bp 3'