Canonical Allele Identifier: CA118324602
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs768413675

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645131C>G , CM000667.2:g.45645131C>G GRCh38
NC_000005.9:g.45645233C>G , CM000667.1:g.45645233C>G GRCh37
NC_000005.8:g.45680990C>G NCBI36
NG_042183.1:g.55988G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.849+54G>C MANE Select ENSP00000307342.4:n.849+54G>C
ENST00000637256.1:n.77+54G>C
ENST00000673735.1:c.849+54G>C ENSP00000501107.1:n.849+54G>C
ENST00000303230.5:c.849+54G>C ENSP00000307342.4:n.849+54G>C
ENST00000634658.1:c.*15G>C ENSP00000489134.1:n.*15G>C
NM_021072.3:c.849+54G>C NP_066550.2:n.849+54G>C
NM_021072.4:c.849+54G>C MANE Select NP_066550.2:n.849+54G>C