Canonical Allele Identifier: CA7648847
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs760167555
ExAC: 15:73615115 GC / G
gnomAD v2: 15-73615115-GC-G
MyVariant Identifiers: chr15:g.73615116del (hg19) chr15:g.73322775del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322775del , CM000677.2:g.73322775del GRCh38
NC_000015.9:g.73615116del , CM000677.1:g.73615116del GRCh37
NC_000015.8:g.71402169del NCBI36
NG_009063.1:g.51490del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3318del MANE Select ENSP00000261917.3:p.His1107ThrfsTer?
ENST00000261917.3:c.3318del ENSP00000261917.3:p.His1107ThrfsTer?
NM_005477.2:c.3318del NP_005468.1:p.His1107ThrfsTer?
XM_011521148.1:c.2100del XP_011519450.1:p.His701ThrfsTer?
XM_011521148.2:c.2100del XP_011519450.1:p.His701ThrfsTer?
NM_005477.3:c.3318del MANE Select NP_005468.1:p.His1107ThrfsTer?
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