Canonical Allele Identifier: CA1543688766
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs894060664
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45462280G>C , CM000667.2:g.45462280G>C GRCh38
NC_000005.9:g.45462382G>C , CM000667.1:g.45462382G>C GRCh37
NC_000005.8:g.45498139G>C NCBI36
NG_042183.1:g.238839C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.850-273C>G MANE Select ENSP00000307342.4:n.850-273C>G
ENST00000637305.1:n.13-273C>G
ENST00000673735.1:c.850-273C>G ENSP00000501107.1:n.850-273C>G
ENST00000303230.5:c.850-273C>G ENSP00000307342.4:n.850-273C>G
NM_021072.3:c.850-273C>G NP_066550.2:n.850-273C>G
NM_021072.4:c.850-273C>G MANE Select NP_066550.2:n.850-273C>G
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