Canonical Allele Identifier: CA359704775
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461877G>C , CM000667.2:g.45461877G>C GRCh38
NC_000005.9:g.45461979G>C , CM000667.1:g.45461979G>C GRCh37
NC_000005.8:g.45497736G>C NCBI36
NG_042183.1:g.239242C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.980C>G MANE Select ENSP00000307342.4:p.Pro327Arg
ENST00000637305.1:n.143C>G
ENST00000673735.1:c.980C>G ENSP00000501107.1:p.Pro327Arg
ENST00000303230.5:c.980C>G ENSP00000307342.4:p.Pro327Arg
NM_021072.3:c.980C>G NP_066550.2:p.Pro327Arg
NM_021072.4:c.980C>G MANE Select NP_066550.2:p.Pro327Arg