Canonical Allele Identifier: CA359704847
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461892A>T , CM000667.2:g.45461892A>T GRCh38
NC_000005.9:g.45461994A>T , CM000667.1:g.45461994A>T GRCh37
NC_000005.8:g.45497751A>T NCBI36
NG_042183.1:g.239227T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.965T>A MANE Select ENSP00000307342.4:p.Leu322Gln
ENST00000637305.1:n.128T>A
ENST00000673735.1:c.965T>A ENSP00000501107.1:p.Leu322Gln
ENST00000303230.5:c.965T>A ENSP00000307342.4:p.Leu322Gln
NM_021072.3:c.965T>A NP_066550.2:p.Leu322Gln
NM_021072.4:c.965T>A MANE Select NP_066550.2:p.Leu322Gln