Canonical Allele Identifier: CA491478270
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1077810
ClinVar RCV Id: RCV001392489
dbSNP Id: rs1372157927
gnomAD v4: 15-73323600-G-A
MyVariant Identifiers: chr15:g.73615941G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323600G>A , CM000677.2:g.73323600G>A GRCh38
NC_000015.9:g.73615941G>A , CM000677.1:g.73615941G>A GRCh37
NC_000015.8:g.71402994G>A NCBI36
NG_009063.1:g.50665C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2493C>T MANE Select ENSP00000261917.3:p.Ser831=
ENST00000261917.3:c.2493C>T ENSP00000261917.3:p.Ser831=
NM_005477.2:c.2493C>T NP_005468.1:p.Ser831=
XM_011521148.1:c.1275C>T XP_011519450.1:p.Ser425=
XM_011521148.2:c.1275C>T XP_011519450.1:p.Ser425=
NM_005477.3:c.2493C>T MANE Select NP_005468.1:p.Ser831=
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