Canonical Allele Identifier: CA2187167860

Gene: HCN4

Linked Data

• dbSNP Id: rs2042923297

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73330003del , CM000677.2:g.73330003del	GRCh38
NC_000015.9:g.73622344del , CM000677.1:g.73622344del	GRCh37
NC_000015.8:g.71409397del	NCBI36
NG_009063.1:g.44266del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1372-208del MANE Select	ENSP00000261917.3:n.1372-208del
ENST00000261917.3:c.1372-208del	ENSP00000261917.3:n.1372-208del
NM_005477.2:c.1372-208del	NP_005468.1:n.1372-208del
XM_011521148.1:c.154-208del	XP_011519450.1:n.154-208del
XM_011521148.2:c.154-208del	XP_011519450.1:n.154-208del
NM_005477.3:c.1372-208del MANE Select	NP_005468.1:n.1372-208del