Canonical Allele Identifier: CA491479610

Gene: HCN4

Linked Data

• ClinVar Variation Id: 1743904
• ClinVar RCV Id: RCV002340586 ; RCV003505232
• dbSNP Id: rs1262527275
• gnomAD v2: 15-73660123-G-A
• gnomAD v3: 15-73367782-G-A
• gnomAD v4: 15-73367782-G-A
• MyVariant Identifiers: chr15:g.73660123G>A (hg19) ; chr15:g.73367782G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367782G>A , CM000677.2:g.73367782G>A	GRCh38
NC_000015.9:g.73660123G>A , CM000677.1:g.73660123G>A	GRCh37
NC_000015.8:g.71447176G>A	NCBI36
NG_009063.1:g.6483C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.489C>T MANE Select	ENSP00000261917.3:p.Ala163=
ENST00000261917.3:c.489C>T	ENSP00000261917.3:p.Ala163=
NM_005477.2:c.489C>T	NP_005468.1:p.Ala163=
NM_005477.3:c.489C>T MANE Select	NP_005468.1:p.Ala163=