Canonical Allele Identifier: CA272684408
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 660645
ClinVar RCV Id: RCV000817888 RCV004028929
dbSNP Id: rs918783630
gnomAD v4: 15-73343426-G-A
COSMIC: COSM964680
MyVariant Identifiers: chr15:g.73635767G>A (hg19) chr15:g.73343426G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343426G>A , CM000677.2:g.73343426G>A GRCh38
NC_000015.9:g.73635767G>A , CM000677.1:g.73635767G>A GRCh37
NC_000015.8:g.71422820G>A NCBI36
NG_009063.1:g.30839C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1168C>T MANE Select ENSP00000261917.3:p.Arg390Cys
ENST00000261917.3:c.1168C>T ENSP00000261917.3:p.Arg390Cys
NM_005477.2:c.1168C>T NP_005468.1:p.Arg390Cys
NM_005477.3:c.1168C>T MANE Select NP_005468.1:p.Arg390Cys
Search 100 bp 5'
Search 100 bp 3'