Canonical Allele Identifier: CA491478571
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626622
ClinVar RCV Id: RCV003384162
dbSNP Id: rs1447571299
gnomAD v2: 15-73615764-G-T
gnomAD v4: 15-73323423-G-T
MyVariant Identifiers: chr15:g.73615764G>T (hg19) chr15:g.73323423G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323423G>T , CM000677.2:g.73323423G>T GRCh38
NC_000015.9:g.73615764G>T , CM000677.1:g.73615764G>T GRCh37
NC_000015.8:g.71402817G>T NCBI36
NG_009063.1:g.50842C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2670C>A MANE Select ENSP00000261917.3:p.Pro890=
ENST00000261917.3:c.2670C>A ENSP00000261917.3:p.Pro890=
NM_005477.2:c.2670C>A NP_005468.1:p.Pro890=
XM_011521148.1:c.1452C>A XP_011519450.1:p.Pro484=
XM_011521148.2:c.1452C>A XP_011519450.1:p.Pro484=
NM_005477.3:c.2670C>A MANE Select NP_005468.1:p.Pro890=
Search 100 bp 5'
Search 100 bp 3'