Canonical Allele Identifier: CA359704980
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45462049T>C (hg19) chr5:g.45461947T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461947T>C , CM000667.2:g.45461947T>C GRCh38
NC_000005.9:g.45462049T>C , CM000667.1:g.45462049T>C GRCh37
NC_000005.8:g.45497806T>C NCBI36
NG_042183.1:g.239172A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.910A>G MANE Select ENSP00000307342.4:p.Met304Val
ENST00000637305.1:n.73A>G
ENST00000673735.1:c.910A>G ENSP00000501107.1:p.Met304Val
ENST00000303230.5:c.910A>G ENSP00000307342.4:p.Met304Val
NM_021072.3:c.910A>G NP_066550.2:p.Met304Val
NM_021072.4:c.910A>G MANE Select NP_066550.2:p.Met304Val
Search 100 bp 5'
Search 100 bp 3'