Canonical Allele Identifier: CA10604722
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 284202
ClinVar RCV Id: RCV000396337
dbSNP Id: rs886042821
MyVariant Identifiers: chr15:g.73622042C>T (hg19) chr15:g.73329701C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329701C>T , CM000677.2:g.73329701C>T GRCh38
NC_000015.9:g.73622042C>T , CM000677.1:g.73622042C>T GRCh37
NC_000015.8:g.71409095C>T NCBI36
NG_009063.1:g.44564G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1462G>A MANE Select ENSP00000261917.3:p.Gly488Ser
ENST00000261917.3:c.1462G>A ENSP00000261917.3:p.Gly488Ser
NM_005477.2:c.1462G>A NP_005468.1:p.Gly488Ser
XM_011521148.1:c.244G>A XP_011519450.1:p.Gly82Ser
XM_011521148.2:c.244G>A XP_011519450.1:p.Gly82Ser
NM_005477.3:c.1462G>A MANE Select NP_005468.1:p.Gly488Ser
Search 100 bp 5'
Search 100 bp 3'