Canonical Allele Identifier: CA971406375

Gene: HCN4

Linked Data

• dbSNP Id: rs2042924118
• gnomAD v3: 15-73330096-A-AGGCCCCG
• gnomAD v4: 15-73330096-A-AGGCCCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73330100_73330106dup , CM000677.2:g.73330100_73330106dup	GRCh38
NC_000015.9:g.73622441_73622447dup , CM000677.1:g.73622441_73622447dup	GRCh37
NC_000015.8:g.71409494_71409500dup	NCBI36
NG_009063.1:g.44162_44168dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1372-312_1372-306dup MANE Select	ENSP00000261917.3:n.1372-312_1372-306dup
ENST00000261917.3:c.1372-312_1372-306dup	ENSP00000261917.3:n.1372-312_1372-306dup
NM_005477.2:c.1372-312_1372-306dup	NP_005468.1:n.1372-312_1372-306dup
XM_011521148.1:c.154-312_154-306dup	XP_011519450.1:n.154-312_154-306dup
XM_011521148.2:c.154-312_154-306dup	XP_011519450.1:n.154-312_154-306dup
NM_005477.3:c.1372-312_1372-306dup MANE Select	NP_005468.1:n.1372-312_1372-306dup