Canonical Allele Identifier: CA2187185887
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042864651
gnomAD v4: 15-73322394-TA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322395del , CM000677.2:g.73322395del GRCh38
NC_000015.9:g.73614736del , CM000677.1:g.73614736del GRCh37
NC_000015.8:g.71401789del NCBI36
NG_009063.1:g.51870del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*86del MANE Select ENSP00000261917.3:n.*86del
ENST00000261917.3:c.*86del ENSP00000261917.3:n.*86del
NM_005477.2:c.*86del NP_005468.1:n.*86del
XM_011521148.1:c.*86del XP_011519450.1:n.*86del
XM_011521148.2:c.*86del XP_011519450.1:n.*86del
NM_005477.3:c.*86del MANE Select NP_005468.1:n.*86del
Search 100 bp 5'
Search 100 bp 3'