Canonical Allele Identifier: CA1543790882
Gene: HCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645664C= , CM000667.2:g.45645664C= GRCh38
NC_000005.9:g.45645766C= , CM000667.1:g.45645766C= GRCh37
NC_000005.8:g.45681523C= NCBI36
NG_042183.1:g.55455G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.426-56G= MANE Select ENSP00000307342.4:n.426-56G=
ENST00000673735.1:c.426-56G= ENSP00000501107.1:n.426-56G=
ENST00000303230.5:c.426-56G= ENSP00000307342.4:n.426-56G=
ENST00000634658.1:c.426-56G= ENSP00000489134.1:n.426-56G=
NM_021072.3:c.426-56G= NP_066550.2:n.426-56G=
NM_021072.4:c.426-56G= MANE Select NP_066550.2:n.426-56G=
Search 100 bp 5'
Search 100 bp 3'