Canonical Allele Identifier: CA1543688422
Gene: HCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461983C= , CM000667.2:g.45461983C= GRCh38
NC_000005.9:g.45462085C= , CM000667.1:g.45462085C= GRCh37
NC_000005.8:g.45497842C= NCBI36
NG_042183.1:g.239136G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.874G= MANE Select ENSP00000307342.4:p.Ala292=
ENST00000637305.1:n.37G=
ENST00000673735.1:c.874G= ENSP00000501107.1:p.Ala292=
ENST00000303230.5:c.874G= ENSP00000307342.4:p.Ala292=
NM_021072.3:c.874G= NP_066550.2:p.Ala292=
NM_021072.4:c.874G= MANE Select NP_066550.2:p.Ala292=
Search 100 bp 5'
Search 100 bp 3'