Canonical Allele Identifier: CA715542284
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1208406016
gnomAD v3: 15-73322419-TA-T
gnomAD v4: 15-73322419-TA-T
MyVariant Identifiers: chr15:g.73614761del (hg19) chr15:g.73322420del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322422del , CM000677.2:g.73322422del GRCh38
NC_000015.9:g.73614763del , CM000677.1:g.73614763del GRCh37
NC_000015.8:g.71401816del NCBI36
NG_009063.1:g.51845del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*61del MANE Select ENSP00000261917.3:n.*61del
ENST00000261917.3:c.*61del ENSP00000261917.3:n.*61del
NM_005477.2:c.*61del NP_005468.1:n.*61del
XM_011521148.1:c.*61del XP_011519450.1:n.*61del
XM_011521148.2:c.*61del XP_011519450.1:n.*61del
NM_005477.3:c.*61del MANE Select NP_005468.1:n.*61del
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