Canonical Allele Identifier: CA491478314
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 518131
ClinVar RCV Id: RCV000611077 RCV002531720
dbSNP Id: rs1297073936
gnomAD v4: 15-73323348-A-T
MyVariant Identifiers: chr15:g.73615689A>T (hg19) chr15:g.73323348A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323348A>T , CM000677.2:g.73323348A>T GRCh38
NC_000015.9:g.73615689A>T , CM000677.1:g.73615689A>T GRCh37
NC_000015.8:g.71402742A>T NCBI36
NG_009063.1:g.50917T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2745T>A MANE Select ENSP00000261917.3:p.Gly915=
ENST00000261917.3:c.2745T>A ENSP00000261917.3:p.Gly915=
NM_005477.2:c.2745T>A NP_005468.1:p.Gly915=
XM_011521148.1:c.1527T>A XP_011519450.1:p.Gly509=
XM_011521148.2:c.1527T>A XP_011519450.1:p.Gly509=
NM_005477.3:c.2745T>A MANE Select NP_005468.1:p.Gly915=
Search 100 bp 5'
Search 100 bp 3'