Canonical Allele Identifier: CA272671989
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1425387
ClinVar RCV Id: RCV001926599
dbSNP Id: rs1040178011
gnomAD v3: 15-73329567-A-T
gnomAD v4: 15-73329567-A-T
MyVariant Identifiers: chr15:g.73621908A>T (hg19) chr15:g.73329567A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329567A>T , CM000677.2:g.73329567A>T GRCh38
NC_000015.9:g.73621908A>T , CM000677.1:g.73621908A>T GRCh37
NC_000015.8:g.71408961A>T NCBI36
NG_009063.1:g.44698T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1590+6T>A MANE Select ENSP00000261917.3:n.1590+6T>A
ENST00000261917.3:c.1590+6T>A ENSP00000261917.3:n.1590+6T>A
NM_005477.2:c.1590+6T>A NP_005468.1:n.1590+6T>A
XM_011521148.1:c.372+6T>A XP_011519450.1:n.372+6T>A
XM_011521148.2:c.372+6T>A XP_011519450.1:n.372+6T>A
NM_005477.3:c.1590+6T>A MANE Select NP_005468.1:n.1590+6T>A
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