Canonical Allele Identifier: CA393097953

Gene: HCN4

Linked Data

• ClinVar Variation Id: 1741871
• ClinVar RCV Id: RCV002342438
• gnomAD v4: 15-73367811-G-A
• MyVariant Identifiers: chr15:g.73660152G>A (hg19) ; chr15:g.73367811G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367811G>A , CM000677.2:g.73367811G>A	GRCh38
NC_000015.9:g.73660152G>A , CM000677.1:g.73660152G>A	GRCh37
NC_000015.8:g.71447205G>A	NCBI36
NG_009063.1:g.6454C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.460C>T MANE Select	ENSP00000261917.3:p.Arg154Cys
ENST00000261917.3:c.460C>T	ENSP00000261917.3:p.Arg154Cys
NM_005477.2:c.460C>T	NP_005468.1:p.Arg154Cys
NM_005477.3:c.460C>T MANE Select	NP_005468.1:p.Arg154Cys