Canonical Allele Identifier: CA359707851
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645568T>A , CM000667.2:g.45645568T>A GRCh38
NC_000005.9:g.45645670T>A , CM000667.1:g.45645670T>A GRCh37
NC_000005.8:g.45681427T>A NCBI36
NG_042183.1:g.55551A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.466A>T MANE Select ENSP00000307342.4:p.Asn156Tyr
ENST00000673735.1:c.466A>T ENSP00000501107.1:p.Asn156Tyr
ENST00000303230.5:c.466A>T ENSP00000307342.4:p.Asn156Tyr
ENST00000634658.1:c.466A>T ENSP00000489134.1:p.Asn156Tyr
NM_021072.3:c.466A>T NP_066550.2:p.Asn156Tyr
NM_021072.4:c.466A>T MANE Select NP_066550.2:p.Asn156Tyr