Canonical Allele Identifier: CA811095561
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1334099008
gnomAD v3: 5-45462268-T-C
gnomAD v4: 5-45462268-T-C
MyVariant Identifiers: chr5:g.45462370T>C (hg19) chr5:g.45462268T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45462268T>C , CM000667.2:g.45462268T>C GRCh38
NC_000005.9:g.45462370T>C , CM000667.1:g.45462370T>C GRCh37
NC_000005.8:g.45498127T>C NCBI36
NG_042183.1:g.238851A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.850-261A>G MANE Select ENSP00000307342.4:n.850-261A>G
ENST00000637305.1:n.13-261A>G
ENST00000673735.1:c.850-261A>G ENSP00000501107.1:n.850-261A>G
ENST00000303230.5:c.850-261A>G ENSP00000307342.4:n.850-261A>G
NM_021072.3:c.850-261A>G NP_066550.2:n.850-261A>G
NM_021072.4:c.850-261A>G MANE Select NP_066550.2:n.850-261A>G
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