Canonical Allele Identifier: CA2187185881
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042864622
gnomAD v4: 15-73322384-TTATTACTGTTATTGG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322388_73322402del , CM000677.2:g.73322388_73322402del GRCh38
NC_000015.9:g.73614729_73614743del , CM000677.1:g.73614729_73614743del GRCh37
NC_000015.8:g.71401782_71401796del NCBI36
NG_009063.1:g.51866_51880del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*82_*96del MANE Select ENSP00000261917.3:n.*82_*96del
ENST00000261917.3:c.*82_*96del ENSP00000261917.3:n.*82_*96del
NM_005477.2:c.*82_*96del NP_005468.1:n.*82_*96del
XM_011521148.1:c.*82_*96del XP_011519450.1:n.*82_*96del
XM_011521148.2:c.*82_*96del XP_011519450.1:n.*82_*96del
NM_005477.3:c.*82_*96del MANE Select NP_005468.1:n.*82_*96del
Search 100 bp 5'
Search 100 bp 3'