Canonical Allele Identifier: CA2317212829
Gene: HCN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.616000G= , CM000681.2:g.616000G= GRCh38
NC_000019.9:g.616000G= , CM000681.1:g.616000G= GRCh37
NC_000019.8:g.567000G= NCBI36
NG_023049.1:g.22569C=
NG_052810.1:g.31108G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2196G= MANE Select ENSP00000251287.1:p.Gln732=
ENST00000251287.2:c.2196G= ENSP00000251287.1:p.Gln732=
NM_001194.3:c.2196G= NP_001185.3:p.Gln732=
NM_001194.4:c.2196G= MANE Select NP_001185.3:p.Gln732=
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