Canonical Allele Identifier: CA504875744
Gene: HCN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.616009C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.616009C>G , CM000681.2:g.616009C>G GRCh38
NC_000019.9:g.616009C>G , CM000681.1:g.616009C>G GRCh37
NC_000019.8:g.567009C>G NCBI36
NG_023049.1:g.22560G>C
NG_052810.1:g.31117C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2205C>G MANE Select ENSP00000251287.1:p.Ala735=
ENST00000251287.2:c.2205C>G ENSP00000251287.1:p.Ala735=
NM_001194.3:c.2205C>G NP_001185.3:p.Ala735=
NM_001194.4:c.2205C>G MANE Select NP_001185.3:p.Ala735=
Search 100 bp 5'
Search 100 bp 3'