Canonical Allele Identifier: CA272700334

Gene: HCN4

Linked Data

• ClinVar Variation Id: 579994
• ClinVar RCV Id: RCV000703412 ; RCV002334371 ; RCV002493234
• dbSNP Id: rs924203370
• gnomAD v2: 15-73660146-C-T
• gnomAD v3: 15-73367805-C-T
• gnomAD v4: 15-73367805-C-T
• MyVariant Identifiers: chr15:g.73660146C>T (hg19) ; chr15:g.73367805C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367805C>T , CM000677.2:g.73367805C>T	GRCh38
NC_000015.9:g.73660146C>T , CM000677.1:g.73660146C>T	GRCh37
NC_000015.8:g.71447199C>T	NCBI36
NG_009063.1:g.6460G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.466G>A MANE Select	ENSP00000261917.3:p.Gly156Ser
ENST00000261917.3:c.466G>A	ENSP00000261917.3:p.Gly156Ser
NM_005477.2:c.466G>A	NP_005468.1:p.Gly156Ser
NM_005477.3:c.466G>A MANE Select	NP_005468.1:p.Gly156Ser