Canonical Allele Identifier: CA7648835
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 945339
ClinVar RCV Id: RCV001215959 RCV002451475
dbSNP Id: rs532186403
ExAC: 15:73615037 C / T
gnomAD v2: 15-73615037-C-T
gnomAD v4: 15-73322696-C-T
MyVariant Identifiers: chr15:g.73615037C>T (hg19) chr15:g.73322696C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322696C>T , CM000677.2:g.73322696C>T GRCh38
NC_000015.9:g.73615037C>T , CM000677.1:g.73615037C>T GRCh37
NC_000015.8:g.71402090C>T NCBI36
NG_009063.1:g.51569G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3397G>A MANE Select ENSP00000261917.3:p.Gly1133Arg
ENST00000261917.3:c.3397G>A ENSP00000261917.3:p.Gly1133Arg
NM_005477.2:c.3397G>A NP_005468.1:p.Gly1133Arg
XM_011521148.1:c.2179G>A XP_011519450.1:p.Gly727Arg
XM_011521148.2:c.2179G>A XP_011519450.1:p.Gly727Arg
NM_005477.3:c.3397G>A MANE Select NP_005468.1:p.Gly1133Arg
Search 100 bp 5'
Search 100 bp 3'