Canonical Allele Identifier: CA2629389821

Gene: HCN4

Linked Data

• gnomAD v4: 15-73367833-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367838dup , CM000677.2:g.73367838dup	GRCh38
NC_000015.9:g.73660179dup , CM000677.1:g.73660179dup	GRCh37
NC_000015.8:g.71447232dup	NCBI36
NG_009063.1:g.6431dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.437dup MANE Select	ENSP00000261917.3:p.Gly147ArgfsTer?
ENST00000261917.3:c.437dup	ENSP00000261917.3:p.Gly147ArgfsTer?
NM_005477.2:c.437dup	NP_005468.1:p.Gly147ArgfsTer?
NM_005477.3:c.437dup MANE Select	NP_005468.1:p.Gly147ArgfsTer?