Canonical Allele Identifier: CA359706973
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45645286C>T (hg19) chr5:g.45645184C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645184C>T , CM000667.2:g.45645184C>T GRCh38
NC_000005.9:g.45645286C>T , CM000667.1:g.45645286C>T GRCh37
NC_000005.8:g.45681043C>T NCBI36
NG_042183.1:g.55935G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.849+1G>A MANE Select ENSP00000307342.4:n.849+1G>A
ENST00000637256.1:n.77+1G>A
ENST00000673735.1:c.849+1G>A ENSP00000501107.1:n.849+1G>A
ENST00000303230.5:c.849+1G>A ENSP00000307342.4:n.849+1G>A
ENST00000634658.1:c.850G>A ENSP00000489134.1:p.Val284Ile
NM_021072.3:c.849+1G>A NP_066550.2:n.849+1G>A
NM_021072.4:c.849+1G>A MANE Select NP_066550.2:n.849+1G>A
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