Canonical Allele Identifier: CA7649050
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs777815693
ExAC: 15:73616124 CGTG / C
gnomAD v2: 15-73616124-CGTG-C
MyVariant Identifiers: chr15:g.73616125_73616127del (hg19) chr15:g.73323784_73323786del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323785_73323787del , CM000677.2:g.73323785_73323787del GRCh38
NC_000015.9:g.73616126_73616128del , CM000677.1:g.73616126_73616128del GRCh37
NC_000015.8:g.71403179_71403181del NCBI36
NG_009063.1:g.50479_50481del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2307_2309del MANE Select ENSP00000261917.3:p.Thr770del
ENST00000261917.3:c.2307_2309del ENSP00000261917.3:p.Thr770del
NM_005477.2:c.2307_2309del NP_005468.1:p.Thr770del
XM_011521148.1:c.1089_1091del XP_011519450.1:p.Thr364del
XM_011521148.2:c.1089_1091del XP_011519450.1:p.Thr364del
NM_005477.3:c.2307_2309del MANE Select NP_005468.1:p.Thr770del
Search 100 bp 5'
Search 100 bp 3'