Canonical Allele Identifier: CA2317212744
Gene: HCN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.615890A= , CM000681.2:g.615890A= GRCh38
NC_000019.9:g.615890A= , CM000681.1:g.615890A= GRCh37
NC_000019.8:g.566890A= NCBI36
NG_023049.1:g.22679T=
NG_052810.1:g.30998A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2086A= MANE Select ENSP00000251287.1:p.Lys696=
ENST00000251287.2:c.2086A= ENSP00000251287.1:p.Lys696=
NM_001194.3:c.2086A= NP_001185.3:p.Lys696=
NM_001194.4:c.2086A= MANE Select NP_001185.3:p.Lys696=
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