Canonical Allele Identifier: CA359705051
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461979C>T , CM000667.2:g.45461979C>T GRCh38
NC_000005.9:g.45462081C>T , CM000667.1:g.45462081C>T GRCh37
NC_000005.8:g.45497838C>T NCBI36
NG_042183.1:g.239140G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.878G>A MANE Select ENSP00000307342.4:p.Ser293Asn
ENST00000637305.1:n.41G>A
ENST00000673735.1:c.878G>A ENSP00000501107.1:p.Ser293Asn
ENST00000303230.5:c.878G>A ENSP00000307342.4:p.Ser293Asn
NM_021072.3:c.878G>A NP_066550.2:p.Ser293Asn
NM_021072.4:c.878G>A MANE Select NP_066550.2:p.Ser293Asn