Canonical Allele Identifier: CA444258213
Gene: HCN1 HGNC NCBI

Linked Data

gnomAD v3: 5-45461957-A-G
gnomAD v4: 5-45461957-A-G
MyVariant Identifiers: chr5:g.45462059A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461957A>G , CM000667.2:g.45461957A>G GRCh38
NC_000005.9:g.45462059A>G , CM000667.1:g.45462059A>G GRCh37
NC_000005.8:g.45497816A>G NCBI36
NG_042183.1:g.239162T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.900T>C MANE Select ENSP00000307342.4:p.Asn300=
ENST00000637305.1:n.63T>C
ENST00000673735.1:c.900T>C ENSP00000501107.1:p.Asn300=
ENST00000303230.5:c.900T>C ENSP00000307342.4:p.Asn300=
NM_021072.3:c.900T>C NP_066550.2:p.Asn300=
NM_021072.4:c.900T>C MANE Select NP_066550.2:p.Asn300=