Canonical Allele Identifier: CA393097365
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 838216
ClinVar RCV Id: RCV001039723
dbSNP Id: rs912161486
MyVariant Identifiers: chr15:g.73659966G>C (hg19) chr15:g.73367625G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367625G>C , CM000677.2:g.73367625G>C GRCh38
NC_000015.9:g.73659966G>C , CM000677.1:g.73659966G>C GRCh37
NC_000015.8:g.71447019G>C NCBI36
NG_009063.1:g.6640C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.646C>G MANE Select ENSP00000261917.3:p.Arg216Gly
ENST00000261917.3:c.646C>G ENSP00000261917.3:p.Arg216Gly
NM_005477.2:c.646C>G NP_005468.1:p.Arg216Gly
NM_005477.3:c.646C>G MANE Select NP_005468.1:p.Arg216Gly
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