Canonical Allele Identifier: CA7649276
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs769526558
ExAC: 15:73621920 CT / C
gnomAD v2: 15-73621920-CT-C
gnomAD v4: 15-73329579-CT-C
MyVariant Identifiers: chr15:g.73621921del (hg19) chr15:g.73329580del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329580del , CM000677.2:g.73329580del GRCh38
NC_000015.9:g.73621921del , CM000677.1:g.73621921del GRCh37
NC_000015.8:g.71408974del NCBI36
NG_009063.1:g.44685del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1583del MANE Select ENSP00000261917.3:p.Gln528ArgfsTer?
ENST00000261917.3:c.1583del ENSP00000261917.3:p.Gln528ArgfsTer?
NM_005477.2:c.1583del NP_005468.1:p.Gln528ArgfsTer?
XM_011521148.1:c.365del XP_011519450.1:p.Gln122ArgfsTer?
XM_011521148.2:c.365del XP_011519450.1:p.Gln122ArgfsTer?
NM_005477.3:c.1583del MANE Select NP_005468.1:p.Gln528ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'