Canonical Allele Identifier: CA359705081
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45462094A>G (hg19) chr5:g.45461992A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461992A>G , CM000667.2:g.45461992A>G GRCh38
NC_000005.9:g.45462094A>G , CM000667.1:g.45462094A>G GRCh37
NC_000005.8:g.45497851A>G NCBI36
NG_042183.1:g.239127T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.865T>C MANE Select ENSP00000307342.4:p.Tyr289His
ENST00000637305.1:n.28T>C
ENST00000673735.1:c.865T>C ENSP00000501107.1:p.Tyr289His
ENST00000303230.5:c.865T>C ENSP00000307342.4:p.Tyr289His
NM_021072.3:c.865T>C NP_066550.2:p.Tyr289His
NM_021072.4:c.865T>C MANE Select NP_066550.2:p.Tyr289His
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