Canonical Allele Identifier: CA2673782250
Gene: HCN1 HGNC NCBI

Linked Data

gnomAD v4: 5-45645675-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645675A>T , CM000667.2:g.45645675A>T GRCh38
NC_000005.9:g.45645777A>T , CM000667.1:g.45645777A>T GRCh37
NC_000005.8:g.45681534A>T NCBI36
NG_042183.1:g.55444T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.426-67T>A MANE Select ENSP00000307342.4:n.426-67T>A
ENST00000673735.1:c.426-67T>A ENSP00000501107.1:n.426-67T>A
ENST00000303230.5:c.426-67T>A ENSP00000307342.4:n.426-67T>A
ENST00000634658.1:c.426-67T>A ENSP00000489134.1:n.426-67T>A
NM_021072.3:c.426-67T>A NP_066550.2:n.426-67T>A
NM_021072.4:c.426-67T>A MANE Select NP_066550.2:n.426-67T>A
Search 100 bp 5'
Search 100 bp 3'