Canonical Allele Identifier: CA359707492
Gene: HCN1 HGNC NCBI

Linked Data

COSMIC: COSM5403583
MyVariant Identifiers: chr5:g.45645511C>T (hg19) chr5:g.45645409C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645409C>T , CM000667.2:g.45645409C>T GRCh38
NC_000005.9:g.45645511C>T , CM000667.1:g.45645511C>T GRCh37
NC_000005.8:g.45681268C>T NCBI36
NG_042183.1:g.55710G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.625G>A MANE Select ENSP00000307342.4:p.Asp209Asn
ENST00000673735.1:c.625G>A ENSP00000501107.1:p.Asp209Asn
ENST00000303230.5:c.625G>A ENSP00000307342.4:p.Asp209Asn
ENST00000634658.1:c.625G>A ENSP00000489134.1:p.Asp209Asn
NM_021072.3:c.625G>A NP_066550.2:p.Asp209Asn
NM_021072.4:c.625G>A MANE Select NP_066550.2:p.Asp209Asn
Search 100 bp 5'
Search 100 bp 3'