Canonical Allele Identifier: CA1543688776
Gene: HCN1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45462292T= , CM000667.2:g.45462292T= GRCh38
NC_000005.9:g.45462394T= , CM000667.1:g.45462394T= GRCh37
NC_000005.8:g.45498151T= NCBI36
NG_042183.1:g.238827A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.850-285A= MANE Select ENSP00000307342.4:n.850-285A=
ENST00000637305.1:n.13-285A=
ENST00000673735.1:c.850-285A= ENSP00000501107.1:n.850-285A=
ENST00000303230.5:c.850-285A= ENSP00000307342.4:n.850-285A=
NM_021072.3:c.850-285A= NP_066550.2:n.850-285A=
NM_021072.4:c.850-285A= MANE Select NP_066550.2:n.850-285A=
Search 100 bp 5'
Search 100 bp 3'