Canonical Allele Identifier: CA359707834
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1745533150
MyVariant Identifiers: chr5:g.45645661T>C (hg19) chr5:g.45645559T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645559T>C , CM000667.2:g.45645559T>C GRCh38
NC_000005.9:g.45645661T>C , CM000667.1:g.45645661T>C GRCh37
NC_000005.8:g.45681418T>C NCBI36
NG_042183.1:g.55560A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.475A>G MANE Select ENSP00000307342.4:p.Ile159Val
ENST00000673735.1:c.475A>G ENSP00000501107.1:p.Ile159Val
ENST00000303230.5:c.475A>G ENSP00000307342.4:p.Ile159Val
ENST00000634658.1:c.475A>G ENSP00000489134.1:p.Ile159Val
NM_021072.3:c.475A>G NP_066550.2:p.Ile159Val
NM_021072.4:c.475A>G MANE Select NP_066550.2:p.Ile159Val
Search 100 bp 5'
Search 100 bp 3'