Canonical Allele Identifier: CA1543688671
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45462179T= , CM000667.2:g.45462179T= GRCh38
NC_000005.9:g.45462281T= , CM000667.1:g.45462281T= GRCh37
NC_000005.8:g.45498038T= NCBI36
NG_042183.1:g.238940A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.850-172A= MANE Select ENSP00000307342.4:n.850-172A=
ENST00000637305.1:n.13-172A=
ENST00000673735.1:c.850-172A= ENSP00000501107.1:n.850-172A=
ENST00000303230.5:c.850-172A= ENSP00000307342.4:n.850-172A=
NM_021072.3:c.850-172A= NP_066550.2:n.850-172A=
NM_021072.4:c.850-172A= MANE Select NP_066550.2:n.850-172A=