Canonical Allele Identifier: CA491477773
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1616412
ClinVar RCV Id: RCV002084283 RCV003307982
dbSNP Id: rs2042869247
gnomAD v4: 15-73322778-G-A
MyVariant Identifiers: chr15:g.73615119G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322778G>A , CM000677.2:g.73322778G>A GRCh38
NC_000015.9:g.73615119G>A , CM000677.1:g.73615119G>A GRCh37
NC_000015.8:g.71402172G>A NCBI36
NG_009063.1:g.51487C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3315C>T MANE Select ENSP00000261917.3:p.Ser1105=
ENST00000261917.3:c.3315C>T ENSP00000261917.3:p.Ser1105=
NM_005477.2:c.3315C>T NP_005468.1:p.Ser1105=
XM_011521148.1:c.2097C>T XP_011519450.1:p.Ser699=
XM_011521148.2:c.2097C>T XP_011519450.1:p.Ser699=
NM_005477.3:c.3315C>T MANE Select NP_005468.1:p.Ser1105=
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