Canonical Allele Identifier: CA491478139
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1552775
ClinVar RCV Id: RCV002185099
dbSNP Id: rs2151213863
gnomAD v4: 15-73322718-G-C
MyVariant Identifiers: chr15:g.73615059G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322718G>C , CM000677.2:g.73322718G>C GRCh38
NC_000015.9:g.73615059G>C , CM000677.1:g.73615059G>C GRCh37
NC_000015.8:g.71402112G>C NCBI36
NG_009063.1:g.51547C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3375C>G MANE Select ENSP00000261917.3:p.Gly1125=
ENST00000261917.3:c.3375C>G ENSP00000261917.3:p.Gly1125=
NM_005477.2:c.3375C>G NP_005468.1:p.Gly1125=
XM_011521148.1:c.2157C>G XP_011519450.1:p.Gly719=
XM_011521148.2:c.2157C>G XP_011519450.1:p.Gly719=
NM_005477.3:c.3375C>G MANE Select NP_005468.1:p.Gly1125=
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