Canonical Allele Identifier: CA2317212866
Gene: HCN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.616044T= , CM000681.2:g.616044T= GRCh38
NC_000019.9:g.616044T= , CM000681.1:g.616044T= GRCh37
NC_000019.8:g.567044T= NCBI36
NG_023049.1:g.22525A=
NG_052810.1:g.31152T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2240T= MANE Select ENSP00000251287.1:p.Val747=
ENST00000251287.2:c.2240T= ENSP00000251287.1:p.Val747=
NM_001194.3:c.2240T= NP_001185.3:p.Val747=
NM_001194.4:c.2240T= MANE Select NP_001185.3:p.Val747=
Search 100 bp 5'
Search 100 bp 3'