Canonical Allele Identifier: CA491479658
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2726152
ClinVar RCV Id: RCV003506310
dbSNP Id: rs2043136038
gnomAD v3: 15-73367815-G-C
gnomAD v4: 15-73367815-G-C
MyVariant Identifiers: chr15:g.73660156G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367815G>C , CM000677.2:g.73367815G>C GRCh38
NC_000015.9:g.73660156G>C , CM000677.1:g.73660156G>C GRCh37
NC_000015.8:g.71447209G>C NCBI36
NG_009063.1:g.6450C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.456C>G MANE Select ENSP00000261917.3:p.Pro152=
ENST00000261917.3:c.456C>G ENSP00000261917.3:p.Pro152=
NM_005477.2:c.456C>G NP_005468.1:p.Pro152=
NM_005477.3:c.456C>G MANE Select NP_005468.1:p.Pro152=
Search 100 bp 5'
Search 100 bp 3'