Canonical Allele Identifier: CA359707468
Gene: HCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1306863
ClinVar RCV Id: RCV001771043
dbSNP Id: rs2112032121
MyVariant Identifiers: chr5:g.45645501A>T (hg19) chr5:g.45645399A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645399A>T , CM000667.2:g.45645399A>T GRCh38
NC_000005.9:g.45645501A>T , CM000667.1:g.45645501A>T GRCh37
NC_000005.8:g.45681258A>T NCBI36
NG_042183.1:g.55720T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.635T>A MANE Select ENSP00000307342.4:p.Val212Glu
ENST00000673735.1:c.635T>A ENSP00000501107.1:p.Val212Glu
ENST00000303230.5:c.635T>A ENSP00000307342.4:p.Val212Glu
ENST00000634658.1:c.635T>A ENSP00000489134.1:p.Val212Glu
NM_021072.3:c.635T>A NP_066550.2:p.Val212Glu
NM_021072.4:c.635T>A MANE Select NP_066550.2:p.Val212Glu
Search 100 bp 5'
Search 100 bp 3'