Canonical Allele Identifier: CA444258266
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45462083G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461981G>T , CM000667.2:g.45461981G>T GRCh38
NC_000005.9:g.45462083G>T , CM000667.1:g.45462083G>T GRCh37
NC_000005.8:g.45497840G>T NCBI36
NG_042183.1:g.239138C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.876C>A MANE Select ENSP00000307342.4:p.Ala292=
ENST00000637305.1:n.39C>A
ENST00000673735.1:c.876C>A ENSP00000501107.1:p.Ala292=
ENST00000303230.5:c.876C>A ENSP00000307342.4:p.Ala292=
NM_021072.3:c.876C>A NP_066550.2:p.Ala292=
NM_021072.4:c.876C>A MANE Select NP_066550.2:p.Ala292=
Search 100 bp 5'
Search 100 bp 3'