Canonical Allele Identifier: CA359707075
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45645331A>T (hg19) chr5:g.45645229A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645229A>T , CM000667.2:g.45645229A>T GRCh38
NC_000005.9:g.45645331A>T , CM000667.1:g.45645331A>T GRCh37
NC_000005.8:g.45681088A>T NCBI36
NG_042183.1:g.55890T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.805T>A MANE Select ENSP00000307342.4:p.Leu269Ile
ENST00000637256.1:n.33T>A
ENST00000673735.1:c.805T>A ENSP00000501107.1:p.Leu269Ile
ENST00000303230.5:c.805T>A ENSP00000307342.4:p.Leu269Ile
ENST00000634658.1:c.805T>A ENSP00000489134.1:p.Leu269Ile
NM_021072.3:c.805T>A NP_066550.2:p.Leu269Ile
NM_021072.4:c.805T>A MANE Select NP_066550.2:p.Leu269Ile
Search 100 bp 5'
Search 100 bp 3'