Canonical Allele Identifier: CA2708955571
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs2112031535
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645122del , CM000667.2:g.45645122del GRCh38
NC_000005.9:g.45645224del , CM000667.1:g.45645224del GRCh37
NC_000005.8:g.45680981del NCBI36
NG_042183.1:g.55997del

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.849+63del MANE Select ENSP00000307342.4:n.849+63del
ENST00000637256.1:n.77+63del
ENST00000673735.1:c.849+63del ENSP00000501107.1:n.849+63del
ENST00000303230.5:c.849+63del ENSP00000307342.4:n.849+63del
ENST00000634658.1:c.*24del ENSP00000489134.1:n.*24del
NM_021072.3:c.849+63del NP_066550.2:n.849+63del
NM_021072.4:c.849+63del MANE Select NP_066550.2:n.849+63del
Search 100 bp 5'
Search 100 bp 3'