Canonical Allele Identifier: CA359705087
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461995T>C , CM000667.2:g.45461995T>C GRCh38
NC_000005.9:g.45462097T>C , CM000667.1:g.45462097T>C GRCh37
NC_000005.8:g.45497854T>C NCBI36
NG_042183.1:g.239124A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.862A>G MANE Select ENSP00000307342.4:p.Thr288Ala
ENST00000637305.1:n.25A>G
ENST00000673735.1:c.862A>G ENSP00000501107.1:p.Thr288Ala
ENST00000303230.5:c.862A>G ENSP00000307342.4:p.Thr288Ala
NM_021072.3:c.862A>G NP_066550.2:p.Thr288Ala
NM_021072.4:c.862A>G MANE Select NP_066550.2:p.Thr288Ala