Canonical Allele Identifier: CA393093674
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2699432
ClinVar RCV Id: RCV003505525 RCV004366474
MyVariant Identifiers: chr15:g.73621990C>T (hg19) chr15:g.73329649C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329649C>T , CM000677.2:g.73329649C>T GRCh38
NC_000015.9:g.73621990C>T , CM000677.1:g.73621990C>T GRCh37
NC_000015.8:g.71409043C>T NCBI36
NG_009063.1:g.44616G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1514G>A MANE Select ENSP00000261917.3:p.Cys505Tyr
ENST00000261917.3:c.1514G>A ENSP00000261917.3:p.Cys505Tyr
NM_005477.2:c.1514G>A NP_005468.1:p.Cys505Tyr
XM_011521148.1:c.296G>A XP_011519450.1:p.Cys99Tyr
XM_011521148.2:c.296G>A XP_011519450.1:p.Cys99Tyr
NM_005477.3:c.1514G>A MANE Select NP_005468.1:p.Cys505Tyr
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