Canonical Allele Identifier: CA393098096

Gene: HCN4

Linked Data

• ClinVar Variation Id: 1476453
• ClinVar RCV Id: RCV001977955 ; RCV003382767 ; RCV004526892
• dbSNP Id: rs1567801864
• gnomAD v4: 15-73367858-G-T
• MyVariant Identifiers: chr15:g.73660199G>T (hg19) ; chr15:g.73367858G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367858G>T , CM000677.2:g.73367858G>T	GRCh38
NC_000015.9:g.73660199G>T , CM000677.1:g.73660199G>T	GRCh37
NC_000015.8:g.71447252G>T	NCBI36
NG_009063.1:g.6407C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.413C>A MANE Select	ENSP00000261917.3:p.Ser138Tyr
ENST00000261917.3:c.413C>A	ENSP00000261917.3:p.Ser138Tyr
NM_005477.2:c.413C>A	NP_005468.1:p.Ser138Tyr
NM_005477.3:c.413C>A MANE Select	NP_005468.1:p.Ser138Tyr