Canonical Allele Identifier: CA359707802
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645544T>G , CM000667.2:g.45645544T>G GRCh38
NC_000005.9:g.45645646T>G , CM000667.1:g.45645646T>G GRCh37
NC_000005.8:g.45681403T>G NCBI36
NG_042183.1:g.55575A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.490A>C MANE Select ENSP00000307342.4:p.Ile164Leu
ENST00000673735.1:c.490A>C ENSP00000501107.1:p.Ile164Leu
ENST00000303230.5:c.490A>C ENSP00000307342.4:p.Ile164Leu
ENST00000634658.1:c.490A>C ENSP00000489134.1:p.Ile164Leu
NM_021072.3:c.490A>C NP_066550.2:p.Ile164Leu
NM_021072.4:c.490A>C MANE Select NP_066550.2:p.Ile164Leu