Canonical Allele Identifier: CA14940210
Gene: NCF4-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr22:g.36860804G>A
GRCh37 chr22:g.37256846G>A
gnomAD v2:
22:37256846 G / A
gnomAD v3:
22:36860804 G / A
gnomAD v4:
chr22-36860804-G-A
Joint Max Group AF 0.64559653 (EAS)
Genomes Max Group AF 0.64559653 (EAS)
ClinVar Allele:
1260780
ClinVar RCV:
RCV001680449
ClinVar Variation:
1270928
dbSNP:
1883112
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36860804G>A , CM000684.2:g.36860804G>A GRCh38
NC_000022.10:g.37256846G>A , CM000684.1:g.37256846G>A GRCh37
NC_000022.9:g.35586792G>A NCBI36
NG_023400.1:g.4817G>A , LRG_159:g.4817G>A

Transcript Alleles

HGVS Amino-acid Change
NR_147197.1:n.351+9289C>T
Search 100 bp 5'
Search 100 bp 3'