Canonical Allele Identifier: CA402882601
Gene: HCN2 HGNC NCBI

Linked Data

gnomAD v4: 19-613852-A-G
MyVariant Identifiers: chr19:g.613852A>G (hg19) chr19:g.613852A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.613852A>G , CM000681.2:g.613852A>G GRCh38
NC_000019.9:g.613852A>G , CM000681.1:g.613852A>G GRCh37
NC_000019.8:g.564852A>G NCBI36
NG_052810.1:g.28960A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251287.3:c.1826A>G MANE Select ENSP00000251287.1:p.Glu609Gly
ENST00000251287.2:c.1826A>G ENSP00000251287.1:p.Glu609Gly
NM_001194.3:c.1826A>G NP_001185.3:p.Glu609Gly
NM_001194.4:c.1826A>G MANE Select NP_001185.3:p.Glu609Gly
Search 100 bp 5'
Search 100 bp 3'