Canonical Allele Identifier: CA3259392
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs772314753
gnomAD v2: 5-45462050-G-T
gnomAD v4: 5-45461948-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461948G>T , CM000667.2:g.45461948G>T GRCh38
NC_000005.9:g.45462050G>T , CM000667.1:g.45462050G>T GRCh37
NC_000005.8:g.45497807G>T NCBI36
NG_042183.1:g.239171C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.909C>A MANE Select ENSP00000307342.4:p.Gly303=
ENST00000637305.1:n.72C>A
ENST00000673735.1:c.909C>A ENSP00000501107.1:p.Gly303=
ENST00000303230.5:c.909C>A ENSP00000307342.4:p.Gly303=
NM_021072.3:c.909C>A NP_066550.2:p.Gly303=
NM_021072.4:c.909C>A MANE Select NP_066550.2:p.Gly303=