Canonical Allele Identifier: CA491478136
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2915012
ClinVar RCV Id: RCV003615453
dbSNP Id: rs1318015269
gnomAD v2: 15-73615053-C-T
gnomAD v3: 15-73322712-C-T
gnomAD v4: 15-73322712-C-T
MyVariant Identifiers: chr15:g.73615053C>T (hg19) chr15:g.73322712C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322712C>T , CM000677.2:g.73322712C>T GRCh38
NC_000015.9:g.73615053C>T , CM000677.1:g.73615053C>T GRCh37
NC_000015.8:g.71402106C>T NCBI36
NG_009063.1:g.51553G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3381G>A MANE Select ENSP00000261917.3:p.Gly1127=
ENST00000261917.3:c.3381G>A ENSP00000261917.3:p.Gly1127=
NM_005477.2:c.3381G>A NP_005468.1:p.Gly1127=
XM_011521148.1:c.2163G>A XP_011519450.1:p.Gly721=
XM_011521148.2:c.2163G>A XP_011519450.1:p.Gly721=
NM_005477.3:c.3381G>A MANE Select NP_005468.1:p.Gly1127=
Search 100 bp 5'
Search 100 bp 3'