Canonical Allele Identifier: CA1543790158
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1745524989
gnomAD v4: 5-45645134-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645134T>G , CM000667.2:g.45645134T>G GRCh38
NC_000005.9:g.45645236T>G , CM000667.1:g.45645236T>G GRCh37
NC_000005.8:g.45680993T>G NCBI36
NG_042183.1:g.55985A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.849+51A>C MANE Select ENSP00000307342.4:n.849+51A>C
ENST00000637256.1:n.77+51A>C
ENST00000673735.1:c.849+51A>C ENSP00000501107.1:n.849+51A>C
ENST00000303230.5:c.849+51A>C ENSP00000307342.4:n.849+51A>C
ENST00000634658.1:c.*12A>C ENSP00000489134.1:n.*12A>C
NM_021072.3:c.849+51A>C NP_066550.2:n.849+51A>C
NM_021072.4:c.849+51A>C MANE Select NP_066550.2:n.849+51A>C
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