Canonical Allele Identifier: CA393097448

Gene: HCN4

Linked Data

• ClinVar Variation Id: 1752212
• ClinVar RCV Id: RCV002366470
• gnomAD v4: 15-73367651-C-A
• MyVariant Identifiers: chr15:g.73659992C>A (hg19) ; chr15:g.73367651C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367651C>A , CM000677.2:g.73367651C>A	GRCh38
NC_000015.9:g.73659992C>A , CM000677.1:g.73659992C>A	GRCh37
NC_000015.8:g.71447045C>A	NCBI36
NG_009063.1:g.6614G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.620G>T MANE Select	ENSP00000261917.3:p.Arg207Leu
ENST00000261917.3:c.620G>T	ENSP00000261917.3:p.Arg207Leu
NM_005477.2:c.620G>T	NP_005468.1:p.Arg207Leu
NM_005477.3:c.620G>T MANE Select	NP_005468.1:p.Arg207Leu