Canonical Allele Identifier: CA1075706150
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1741174490
gnomAD v3: 5-45462122-TG-T
gnomAD v4: 5-45462122-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45462125del , CM000667.2:g.45462125del GRCh38
NC_000005.9:g.45462227del , CM000667.1:g.45462227del GRCh37
NC_000005.8:g.45497984del NCBI36
NG_042183.1:g.238996del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.850-116del MANE Select ENSP00000307342.4:n.850-116del
ENST00000637305.1:n.13-116del
ENST00000673735.1:c.850-116del ENSP00000501107.1:n.850-116del
ENST00000303230.5:c.850-116del ENSP00000307342.4:n.850-116del
NM_021072.3:c.850-116del NP_066550.2:n.850-116del
NM_021072.4:c.850-116del MANE Select NP_066550.2:n.850-116del
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