Canonical Allele Identifier: CA2317212782
Gene: HCN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.615946_615958delinsCCCGCCGCCGCCG , CM000681.2:g.615946_615958delinsCCCGCCGCCGCCG GRCh38
NC_000019.9:g.615946_615958delinsCCCGCCGCCGCCG , CM000681.1:g.615946_615958delinsCCCGCCGCCGCCG GRCh37
NC_000019.8:g.566946_566958delinsCCCGCCGCCGCCG NCBI36
NG_023049.1:g.22611_22623delinsCGGCGGCGGCGGG
NG_052810.1:g.31054_31066delinsCCCGCCGCCGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2142_2154delinsCCCGCCGCCGCCG MANE Select ENSP00000251287.1:p.Phe714=
ENST00000251287.2:c.2142_2154delinsCCCGCCGCCGCCG ENSP00000251287.1:p.Phe714=
NM_001194.3:c.2142_2154delinsCCCGCCGCCGCCG NP_001185.3:p.Phe714=
NM_001194.4:c.2142_2154delinsCCCGCCGCCGCCG MANE Select NP_001185.3:p.Phe714=
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