Canonical Allele Identifier: CA359704939
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45462031G>C (hg19) chr5:g.45461929G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461929G>C , CM000667.2:g.45461929G>C GRCh38
NC_000005.9:g.45462031G>C , CM000667.1:g.45462031G>C GRCh37
NC_000005.8:g.45497788G>C NCBI36
NG_042183.1:g.239190C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.928C>G MANE Select ENSP00000307342.4:p.His310Asp
ENST00000637305.1:n.91C>G
ENST00000673735.1:c.928C>G ENSP00000501107.1:p.His310Asp
ENST00000303230.5:c.928C>G ENSP00000307342.4:p.His310Asp
NM_021072.3:c.928C>G NP_066550.2:p.His310Asp
NM_021072.4:c.928C>G MANE Select NP_066550.2:p.His310Asp
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