Canonical Allele Identifier: CA359704998
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461956G>A , CM000667.2:g.45461956G>A GRCh38
NC_000005.9:g.45462058G>A , CM000667.1:g.45462058G>A GRCh37
NC_000005.8:g.45497815G>A NCBI36
NG_042183.1:g.239163C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.901C>T MANE Select ENSP00000307342.4:p.Leu301Phe
ENST00000637305.1:n.64C>T
ENST00000673735.1:c.901C>T ENSP00000501107.1:p.Leu301Phe
ENST00000303230.5:c.901C>T ENSP00000307342.4:p.Leu301Phe
NM_021072.3:c.901C>T NP_066550.2:p.Leu301Phe
NM_021072.4:c.901C>T MANE Select NP_066550.2:p.Leu301Phe