Canonical Allele Identifier: CA2578305074
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461749T>A , CM000667.2:g.45461749T>A GRCh38
NC_000005.9:g.45461851T>A , CM000667.1:g.45461851T>A GRCh37
NC_000005.8:g.45497608T>A NCBI36
NG_042183.1:g.239370A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.1011+97A>T MANE Select ENSP00000307342.4:n.1011+97A>T
ENST00000637305.1:n.174+97A>T
ENST00000673735.1:c.1011+97A>T ENSP00000501107.1:n.1011+97A>T
ENST00000303230.5:c.1011+97A>T ENSP00000307342.4:n.1011+97A>T
NM_021072.3:c.1011+97A>T NP_066550.2:n.1011+97A>T
NM_021072.4:c.1011+97A>T MANE Select NP_066550.2:n.1011+97A>T