Canonical Allele Identifier: CA7648839
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 470667
ClinVar RCV Id: RCV000550020 RCV000995388 RCV002456186 RCV002476179
dbSNP Id: rs748279911
ExAC: 15:73615055 C / T
gnomAD v2: 15-73615055-C-T
gnomAD v3: 15-73322714-C-T
gnomAD v4: 15-73322714-C-T
MyVariant Identifiers: chr15:g.73615055C>T (hg19) chr15:g.73322714C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322714C>T , CM000677.2:g.73322714C>T GRCh38
NC_000015.9:g.73615055C>T , CM000677.1:g.73615055C>T GRCh37
NC_000015.8:g.71402108C>T NCBI36
NG_009063.1:g.51551G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3379G>A MANE Select ENSP00000261917.3:p.Gly1127Arg
ENST00000261917.3:c.3379G>A ENSP00000261917.3:p.Gly1127Arg
NM_005477.2:c.3379G>A NP_005468.1:p.Gly1127Arg
XM_011521148.1:c.2161G>A XP_011519450.1:p.Gly721Arg
XM_011521148.2:c.2161G>A XP_011519450.1:p.Gly721Arg
NM_005477.3:c.3379G>A MANE Select NP_005468.1:p.Gly1127Arg
Search 100 bp 5'
Search 100 bp 3'