Canonical Allele Identifier: CA359707407
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645375C>A , CM000667.2:g.45645375C>A GRCh38
NC_000005.9:g.45645477C>A , CM000667.1:g.45645477C>A GRCh37
NC_000005.8:g.45681234C>A NCBI36
NG_042183.1:g.55744G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.659G>T MANE Select ENSP00000307342.4:p.Ser220Ile
ENST00000673735.1:c.659G>T ENSP00000501107.1:p.Ser220Ile
ENST00000303230.5:c.659G>T ENSP00000307342.4:p.Ser220Ile
ENST00000634658.1:c.659G>T ENSP00000489134.1:p.Ser220Ile
NM_021072.3:c.659G>T NP_066550.2:p.Ser220Ile
NM_021072.4:c.659G>T MANE Select NP_066550.2:p.Ser220Ile