Canonical Allele Identifier: CA359705005
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461958T>G , CM000667.2:g.45461958T>G GRCh38
NC_000005.9:g.45462060T>G , CM000667.1:g.45462060T>G GRCh37
NC_000005.8:g.45497817T>G NCBI36
NG_042183.1:g.239161A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.899A>C MANE Select ENSP00000307342.4:p.Asn300Thr
ENST00000637305.1:n.62A>C
ENST00000673735.1:c.899A>C ENSP00000501107.1:p.Asn300Thr
ENST00000303230.5:c.899A>C ENSP00000307342.4:p.Asn300Thr
NM_021072.3:c.899A>C NP_066550.2:p.Asn300Thr
NM_021072.4:c.899A>C MANE Select NP_066550.2:p.Asn300Thr