Canonical Allele Identifier: CA393098529
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1512477
ClinVar RCV Id: RCV002023050 RCV003303644
dbSNP Id: rs746252218
gnomAD v4: 15-73368000-C-G
MyVariant Identifiers: chr15:g.73660341C>G (hg19) chr15:g.73368000C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368000C>G , CM000677.2:g.73368000C>G GRCh38
NC_000015.9:g.73660341C>G , CM000677.1:g.73660341C>G GRCh37
NC_000015.8:g.71447394C>G NCBI36
NG_009063.1:g.6265G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.271G>C MANE Select ENSP00000261917.3:p.Gly91Arg
ENST00000261917.3:c.271G>C ENSP00000261917.3:p.Gly91Arg
NM_005477.2:c.271G>C NP_005468.1:p.Gly91Arg
NM_005477.3:c.271G>C MANE Select NP_005468.1:p.Gly91Arg
Search 100 bp 5'
Search 100 bp 3'