Canonical Allele Identifier: CA1075706179

Gene: HCN1

Linked Data

• dbSNP Id: rs1741178334
• gnomAD v3: 5-45462292-T-A
• gnomAD v4: 5-45462292-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45462292T>A , CM000667.2:g.45462292T>A	GRCh38
NC_000005.9:g.45462394T>A , CM000667.1:g.45462394T>A	GRCh37
NC_000005.8:g.45498151T>A	NCBI36
NG_042183.1:g.238827A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.850-285A>T MANE Select	ENSP00000307342.4:n.850-285A>T
ENST00000637305.1:n.13-285A>T
ENST00000673735.1:c.850-285A>T	ENSP00000501107.1:n.850-285A>T
ENST00000303230.5:c.850-285A>T	ENSP00000307342.4:n.850-285A>T
NM_021072.3:c.850-285A>T	NP_066550.2:n.850-285A>T
NM_021072.4:c.850-285A>T MANE Select	NP_066550.2:n.850-285A>T