Canonical Allele Identifier: CA491479500
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753097
ClinVar RCV Id: RCV002369071
gnomAD v4: 15-73367635-G-C
MyVariant Identifiers: chr15:g.73659976G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367635G>C , CM000677.2:g.73367635G>C GRCh38
NC_000015.9:g.73659976G>C , CM000677.1:g.73659976G>C GRCh37
NC_000015.8:g.71447029G>C NCBI36
NG_009063.1:g.6630C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.636C>G MANE Select ENSP00000261917.3:p.Gly212=
ENST00000261917.3:c.636C>G ENSP00000261917.3:p.Gly212=
NM_005477.2:c.636C>G NP_005468.1:p.Gly212=
NM_005477.3:c.636C>G MANE Select NP_005468.1:p.Gly212=
Search 100 bp 5'
Search 100 bp 3'