Canonical Allele Identifier: CA971406316
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042922812
gnomAD v3: 15-73329897-GC-G
gnomAD v4: 15-73329897-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329898del , CM000677.2:g.73329898del GRCh38
NC_000015.9:g.73622239del , CM000677.1:g.73622239del GRCh37
NC_000015.8:g.71409292del NCBI36
NG_009063.1:g.44367del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-107del MANE Select ENSP00000261917.3:n.1372-107del
ENST00000261917.3:c.1372-107del ENSP00000261917.3:n.1372-107del
NM_005477.2:c.1372-107del NP_005468.1:n.1372-107del
XM_011521148.1:c.154-107del XP_011519450.1:n.154-107del
XM_011521148.2:c.154-107del XP_011519450.1:n.154-107del
NM_005477.3:c.1372-107del MANE Select NP_005468.1:n.1372-107del
Search 100 bp 5'
Search 100 bp 3'