Canonical Allele Identifier: CA402883087
Gene: HCN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.613943C>A (hg19) chr19:g.613943C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.613943C>A , CM000681.2:g.613943C>A GRCh38
NC_000019.9:g.613943C>A , CM000681.1:g.613943C>A GRCh37
NC_000019.8:g.564943C>A NCBI36
NG_052810.1:g.29051C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251287.3:c.1917C>A MANE Select ENSP00000251287.1:p.Asn639Lys
ENST00000251287.2:c.1917C>A ENSP00000251287.1:p.Asn639Lys
NM_001194.3:c.1917C>A NP_001185.3:p.Asn639Lys
NM_001194.4:c.1917C>A MANE Select NP_001185.3:p.Asn639Lys
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