Canonical Allele Identifier: CA402887241
Gene: HCN2 HGNC NCBI

Linked Data

dbSNP Id: rs1983895197
gnomAD v4: 19-616018-C-A
MyVariant Identifiers: chr19:g.616018C>A (hg19) chr19:g.616018C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.616018C>A , CM000681.2:g.616018C>A GRCh38
NC_000019.9:g.616018C>A , CM000681.1:g.616018C>A GRCh37
NC_000019.8:g.567018C>A NCBI36
NG_023049.1:g.22551G>T
NG_052810.1:g.31126C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2214C>A MANE Select ENSP00000251287.1:p.Phe738Leu
ENST00000251287.2:c.2214C>A ENSP00000251287.1:p.Phe738Leu
NM_001194.3:c.2214C>A NP_001185.3:p.Phe738Leu
NM_001194.4:c.2214C>A MANE Select NP_001185.3:p.Phe738Leu
Search 100 bp 5'
Search 100 bp 3'