Canonical Allele Identifier: CA359705090
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461996C>G , CM000667.2:g.45461996C>G GRCh38
NC_000005.9:g.45462098C>G , CM000667.1:g.45462098C>G GRCh37
NC_000005.8:g.45497855C>G NCBI36
NG_042183.1:g.239123G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.861G>C MANE Select ENSP00000307342.4:p.Met287Ile
ENST00000637305.1:n.24G>C
ENST00000673735.1:c.861G>C ENSP00000501107.1:p.Met287Ile
ENST00000303230.5:c.861G>C ENSP00000307342.4:p.Met287Ile
NM_021072.3:c.861G>C NP_066550.2:p.Met287Ile
NM_021072.4:c.861G>C MANE Select NP_066550.2:p.Met287Ile