Canonical Allele Identifier: CA393088774
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2900371
ClinVar RCV Id: RCV003615279
dbSNP Id: rs779148704
gnomAD v2: 15-73615934-G-T
gnomAD v3: 15-73323593-G-T
gnomAD v4: 15-73323593-G-T
MyVariant Identifiers: chr15:g.73615934G>T (hg19) chr15:g.73323593G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323593G>T , CM000677.2:g.73323593G>T GRCh38
NC_000015.9:g.73615934G>T , CM000677.1:g.73615934G>T GRCh37
NC_000015.8:g.71402987G>T NCBI36
NG_009063.1:g.50672C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2500C>A MANE Select ENSP00000261917.3:p.Pro834Thr
ENST00000261917.3:c.2500C>A ENSP00000261917.3:p.Pro834Thr
NM_005477.2:c.2500C>A NP_005468.1:p.Pro834Thr
XM_011521148.1:c.1282C>A XP_011519450.1:p.Pro428Thr
XM_011521148.2:c.1282C>A XP_011519450.1:p.Pro428Thr
NM_005477.3:c.2500C>A MANE Select NP_005468.1:p.Pro834Thr
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