Canonical Allele Identifier: CA1543688351
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461950C= , CM000667.2:g.45461950C= GRCh38
NC_000005.9:g.45462052C= , CM000667.1:g.45462052C= GRCh37
NC_000005.8:g.45497809C= NCBI36
NG_042183.1:g.239169G=

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.907G= MANE Select ENSP00000307342.4:p.Gly303=
ENST00000637305.1:n.70G=
ENST00000673735.1:c.907G= ENSP00000501107.1:p.Gly303=
ENST00000303230.5:c.907G= ENSP00000307342.4:p.Gly303=
NM_021072.3:c.907G= NP_066550.2:p.Gly303=
NM_021072.4:c.907G= MANE Select NP_066550.2:p.Gly303=