Canonical Allele Identifier: CA491480116
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1082754
ClinVar RCV Id: RCV001399151
dbSNP Id: rs1188784278
MyVariant Identifiers: chr15:g.73660585G>C (hg19) chr15:g.73368244G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368244G>C , CM000677.2:g.73368244G>C GRCh38
NC_000015.9:g.73660585G>C , CM000677.1:g.73660585G>C GRCh37
NC_000015.8:g.71447638G>C NCBI36
NG_009063.1:g.6021C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.27C>G MANE Select ENSP00000261917.3:p.Arg9=
ENST00000261917.3:c.27C>G ENSP00000261917.3:p.Arg9=
NM_005477.2:c.27C>G NP_005468.1:p.Arg9=
NM_005477.3:c.27C>G MANE Select NP_005468.1:p.Arg9=
Search 100 bp 5'
Search 100 bp 3'