Canonical Allele Identifier: CA1543688206
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461833A= , CM000667.2:g.45461833A= GRCh38
NC_000005.9:g.45461935A= , CM000667.1:g.45461935A= GRCh37
NC_000005.8:g.45497692A= NCBI36
NG_042183.1:g.239286T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.1011+13T= MANE Select ENSP00000307342.4:n.1011+13T=
ENST00000637305.1:n.174+13T=
ENST00000673735.1:c.1011+13T= ENSP00000501107.1:n.1011+13T=
ENST00000303230.5:c.1011+13T= ENSP00000307342.4:n.1011+13T=
NM_021072.3:c.1011+13T= NP_066550.2:n.1011+13T=
NM_021072.4:c.1011+13T= MANE Select NP_066550.2:n.1011+13T=