Canonical Allele Identifier: CA359707798
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1745532806

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645543A>T , CM000667.2:g.45645543A>T GRCh38
NC_000005.9:g.45645645A>T , CM000667.1:g.45645645A>T GRCh37
NC_000005.8:g.45681402A>T NCBI36
NG_042183.1:g.55576T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.491T>A MANE Select ENSP00000307342.4:p.Ile164Asn
ENST00000673735.1:c.491T>A ENSP00000501107.1:p.Ile164Asn
ENST00000303230.5:c.491T>A ENSP00000307342.4:p.Ile164Asn
ENST00000634658.1:c.491T>A ENSP00000489134.1:p.Ile164Asn
NM_021072.3:c.491T>A NP_066550.2:p.Ile164Asn
NM_021072.4:c.491T>A MANE Select NP_066550.2:p.Ile164Asn