Canonical Allele Identifier: CA359707464
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45645499T>C (hg19) chr5:g.45645397T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645397T>C , CM000667.2:g.45645397T>C GRCh38
NC_000005.9:g.45645499T>C , CM000667.1:g.45645499T>C GRCh37
NC_000005.8:g.45681256T>C NCBI36
NG_042183.1:g.55722A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.637A>G MANE Select ENSP00000307342.4:p.Ile213Val
ENST00000673735.1:c.637A>G ENSP00000501107.1:p.Ile213Val
ENST00000303230.5:c.637A>G ENSP00000307342.4:p.Ile213Val
ENST00000634658.1:c.637A>G ENSP00000489134.1:p.Ile213Val
NM_021072.3:c.637A>G NP_066550.2:p.Ile213Val
NM_021072.4:c.637A>G MANE Select NP_066550.2:p.Ile213Val
Search 100 bp 5'
Search 100 bp 3'