Canonical Allele Identifier: CA2766121171
Gene: HCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645123T>C , CM000667.2:g.45645123T>C GRCh38
NC_000005.9:g.45645225T>C , CM000667.1:g.45645225T>C GRCh37
NC_000005.8:g.45680982T>C NCBI36
NG_042183.1:g.55996A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.849+62A>G MANE Select ENSP00000307342.4:n.849+62A>G
ENST00000637256.1:n.77+62A>G
ENST00000673735.1:c.849+62A>G ENSP00000501107.1:n.849+62A>G
ENST00000303230.5:c.849+62A>G ENSP00000307342.4:n.849+62A>G
ENST00000634658.1:c.*23A>G ENSP00000489134.1:n.*23A>G
NM_021072.3:c.849+62A>G NP_066550.2:n.849+62A>G
NM_021072.4:c.849+62A>G MANE Select NP_066550.2:n.849+62A>G
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