Canonical Allele Identifier: CA393085600
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484271
ClinVar RCV Id: RCV002005669
dbSNP Id: rs2151213893
MyVariant Identifiers: chr15:g.73615106C>T (hg19) chr15:g.73322765C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322765C>T , CM000677.2:g.73322765C>T GRCh38
NC_000015.9:g.73615106C>T , CM000677.1:g.73615106C>T GRCh37
NC_000015.8:g.71402159C>T NCBI36
NG_009063.1:g.51500G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3328G>A MANE Select ENSP00000261917.3:p.Gly1110Arg
ENST00000261917.3:c.3328G>A ENSP00000261917.3:p.Gly1110Arg
NM_005477.2:c.3328G>A NP_005468.1:p.Gly1110Arg
XM_011521148.1:c.2110G>A XP_011519450.1:p.Gly704Arg
XM_011521148.2:c.2110G>A XP_011519450.1:p.Gly704Arg
NM_005477.3:c.3328G>A MANE Select NP_005468.1:p.Gly1110Arg
Search 100 bp 5'
Search 100 bp 3'