Canonical Allele Identifier: CA7649449

Gene: HCN4

Linked Data

• ClinVar Variation Id: 1752277
• ClinVar RCV Id: RCV002366510 ; RCV003098170
• dbSNP Id: rs727503958
• ExAC: 15:73659991 G / A
• gnomAD v2: 15-73659991-G-A
• gnomAD v4: 15-73367650-G-A
• MyVariant Identifiers: chr15:g.73659991G>A (hg19) ; chr15:g.73367650G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367650G>A , CM000677.2:g.73367650G>A	GRCh38
NC_000015.9:g.73659991G>A , CM000677.1:g.73659991G>A	GRCh37
NC_000015.8:g.71447044G>A	NCBI36
NG_009063.1:g.6615C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.621C>T MANE Select	ENSP00000261917.3:p.Arg207=
ENST00000261917.3:c.621C>T	ENSP00000261917.3:p.Arg207=
NM_005477.2:c.621C>T	NP_005468.1:p.Arg207=
NM_005477.3:c.621C>T MANE Select	NP_005468.1:p.Arg207=