Canonical Allele Identifier: CA393098096
Gene: HCN4 HGNC NCBI

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)
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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
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