Canonical Allele Identifier: CA303930507
Gene: HCN2 HGNC NCBI

Linked Data

dbSNP Id: rs756914654

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.615983A>G , CM000681.2:g.615983A>G GRCh38
NC_000019.9:g.615983A>G , CM000681.1:g.615983A>G GRCh37
NC_000019.8:g.566983A>G NCBI36
NG_023049.1:g.22586T>C
NG_052810.1:g.31091A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2179A>G MANE Select ENSP00000251287.1:p.Ile727Val
ENST00000251287.2:c.2179A>G ENSP00000251287.1:p.Ile727Val
NM_001194.3:c.2179A>G NP_001185.3:p.Ile727Val
NM_001194.4:c.2179A>G MANE Select NP_001185.3:p.Ile727Val