Canonical Allele Identifier: CA402886160
Gene: HCN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.615863G>C (hg19) chr19:g.615863G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.615863G>C , CM000681.2:g.615863G>C GRCh38
NC_000019.9:g.615863G>C , CM000681.1:g.615863G>C GRCh37
NC_000019.8:g.566863G>C NCBI36
NG_023049.1:g.22706C>G
NG_052810.1:g.30971G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2059G>C MANE Select ENSP00000251287.1:p.Glu687Gln
ENST00000251287.2:c.2059G>C ENSP00000251287.1:p.Glu687Gln
NM_001194.3:c.2059G>C NP_001185.3:p.Glu687Gln
NM_001194.4:c.2059G>C MANE Select NP_001185.3:p.Glu687Gln
Search 100 bp 5'
Search 100 bp 3'