Canonical Allele Identifier: CA359707680
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45645594G>T (hg19) chr5:g.45645492G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645492G>T , CM000667.2:g.45645492G>T GRCh38
NC_000005.9:g.45645594G>T , CM000667.1:g.45645594G>T GRCh37
NC_000005.8:g.45681351G>T NCBI36
NG_042183.1:g.55627C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.542C>A MANE Select ENSP00000307342.4:p.Ala181Glu
ENST00000673735.1:c.542C>A ENSP00000501107.1:p.Ala181Glu
ENST00000303230.5:c.542C>A ENSP00000307342.4:p.Ala181Glu
ENST00000634658.1:c.542C>A ENSP00000489134.1:p.Ala181Glu
NM_021072.3:c.542C>A NP_066550.2:p.Ala181Glu
NM_021072.4:c.542C>A MANE Select NP_066550.2:p.Ala181Glu
Search 100 bp 5'
Search 100 bp 3'