Canonical Allele Identifier: CA359707668
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645486T>G , CM000667.2:g.45645486T>G GRCh38
NC_000005.9:g.45645588T>G , CM000667.1:g.45645588T>G GRCh37
NC_000005.8:g.45681345T>G NCBI36
NG_042183.1:g.55633A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.548A>C MANE Select ENSP00000307342.4:p.Asp183Ala
ENST00000673735.1:c.548A>C ENSP00000501107.1:p.Asp183Ala
ENST00000303230.5:c.548A>C ENSP00000307342.4:p.Asp183Ala
ENST00000634658.1:c.548A>C ENSP00000489134.1:p.Asp183Ala
NM_021072.3:c.548A>C NP_066550.2:p.Asp183Ala
NM_021072.4:c.548A>C MANE Select NP_066550.2:p.Asp183Ala