Canonical Allele Identifier: CA359707734
Gene: HCN1 HGNC NCBI

Linked Data

gnomAD v4: 5-45645514-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645514G>T , CM000667.2:g.45645514G>T GRCh38
NC_000005.9:g.45645616G>T , CM000667.1:g.45645616G>T GRCh37
NC_000005.8:g.45681373G>T NCBI36
NG_042183.1:g.55605C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.520C>A MANE Select ENSP00000307342.4:p.Pro174Thr
ENST00000673735.1:c.520C>A ENSP00000501107.1:p.Pro174Thr
ENST00000303230.5:c.520C>A ENSP00000307342.4:p.Pro174Thr
ENST00000634658.1:c.520C>A ENSP00000489134.1:p.Pro174Thr
NM_021072.3:c.520C>A NP_066550.2:p.Pro174Thr
NM_021072.4:c.520C>A MANE Select NP_066550.2:p.Pro174Thr