Canonical Allele Identifier: CA393099092

Gene: HCN4

Linked Data

• ClinVar Variation Id: 470675
• ClinVar RCV Id: RCV000532717 ; RCV003403319
• dbSNP Id: rs867068803
• gnomAD v4: 15-73368189-C-T
• MyVariant Identifiers: chr15:g.73660530C>T (hg19) ; chr15:g.73368189C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73368189C>T , CM000677.2:g.73368189C>T	GRCh38
NC_000015.9:g.73660530C>T , CM000677.1:g.73660530C>T	GRCh37
NC_000015.8:g.71447583C>T	NCBI36
NG_009063.1:g.6076G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.82G>A MANE Select	ENSP00000261917.3:p.Glu28Lys
ENST00000261917.3:c.82G>A	ENSP00000261917.3:p.Glu28Lys
NM_005477.2:c.82G>A	NP_005468.1:p.Glu28Lys
NM_005477.3:c.82G>A MANE Select	NP_005468.1:p.Glu28Lys