Canonical Allele Identifier: CA393085091
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732091
ClinVar RCV Id: RCV002459162 RCV003099527
dbSNP Id: rs1374291021
gnomAD v4: 15-73322590-A-C
MyVariant Identifiers: chr15:g.73614931A>C (hg19) chr15:g.73322590A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322590A>C , CM000677.2:g.73322590A>C GRCh38
NC_000015.9:g.73614931A>C , CM000677.1:g.73614931A>C GRCh37
NC_000015.8:g.71401984A>C NCBI36
NG_009063.1:g.51675T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3503T>G MANE Select ENSP00000261917.3:p.Phe1168Cys
ENST00000261917.3:c.3503T>G ENSP00000261917.3:p.Phe1168Cys
NM_005477.2:c.3503T>G NP_005468.1:p.Phe1168Cys
XM_011521148.1:c.2285T>G XP_011519450.1:p.Phe762Cys
XM_011521148.2:c.2285T>G XP_011519450.1:p.Phe762Cys
NM_005477.3:c.3503T>G MANE Select NP_005468.1:p.Phe1168Cys
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