Canonical Allele Identifier: CA359704812
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461884A>T , CM000667.2:g.45461884A>T GRCh38
NC_000005.9:g.45461986A>T , CM000667.1:g.45461986A>T GRCh37
NC_000005.8:g.45497743A>T NCBI36
NG_042183.1:g.239235T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.973T>A MANE Select ENSP00000307342.4:p.Phe325Ile
ENST00000637305.1:n.136T>A
ENST00000673735.1:c.973T>A ENSP00000501107.1:p.Phe325Ile
ENST00000303230.5:c.973T>A ENSP00000307342.4:p.Phe325Ile
NM_021072.3:c.973T>A NP_066550.2:p.Phe325Ile
NM_021072.4:c.973T>A MANE Select NP_066550.2:p.Phe325Ile