Canonical Allele Identifier: CA393085765
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2967411
ClinVar RCV Id: RCV003824089
dbSNP Id: rs1354550200
gnomAD v2: 15-73615144-C-T
gnomAD v4: 15-73322803-C-T
MyVariant Identifiers: chr15:g.73615144C>T (hg19) chr15:g.73322803C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322803C>T , CM000677.2:g.73322803C>T GRCh38
NC_000015.9:g.73615144C>T , CM000677.1:g.73615144C>T GRCh37
NC_000015.8:g.71402197C>T NCBI36
NG_009063.1:g.51462G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3290G>A MANE Select ENSP00000261917.3:p.Gly1097Glu
ENST00000261917.3:c.3290G>A ENSP00000261917.3:p.Gly1097Glu
NM_005477.2:c.3290G>A NP_005468.1:p.Gly1097Glu
XM_011521148.1:c.2072G>A XP_011519450.1:p.Gly691Glu
XM_011521148.2:c.2072G>A XP_011519450.1:p.Gly691Glu
NM_005477.3:c.3290G>A MANE Select NP_005468.1:p.Gly1097Glu
Search 100 bp 5'
Search 100 bp 3'