Canonical Allele Identifier: CA359707660
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645483G>A , CM000667.2:g.45645483G>A GRCh38
NC_000005.9:g.45645585G>A , CM000667.1:g.45645585G>A GRCh37
NC_000005.8:g.45681342G>A NCBI36
NG_042183.1:g.55636C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.551C>T MANE Select ENSP00000307342.4:p.Thr184Ile
ENST00000673735.1:c.551C>T ENSP00000501107.1:p.Thr184Ile
ENST00000303230.5:c.551C>T ENSP00000307342.4:p.Thr184Ile
ENST00000634658.1:c.551C>T ENSP00000489134.1:p.Thr184Ile
NM_021072.3:c.551C>T NP_066550.2:p.Thr184Ile
NM_021072.4:c.551C>T MANE Select NP_066550.2:p.Thr184Ile