Canonical Allele Identifier: CA323557528
Gene: APOL6 HGNC NCBI
MyVariant.info:
GRCh38 chr22:g.35660681G>A
GRCh37 chr22:g.36056728G>A
gnomAD v2:
22:36056728 G / A
gnomAD v3:
22:35660681 G / A
gnomAD v4:
chr22-35660681-G-A
Joint Max Group AF 0.18438962 (EAS)
Genomes Max Group AF 0.18438962 (EAS)
Exomes Max Group AF 0.06716342 (SAS)
dbSNP:
5750146
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35660681G>A , CM000684.2:g.35660681G>A GRCh38
NC_000022.10:g.36056728G>A , CM000684.1:g.36056728G>A GRCh37
NC_000022.9:g.34386674G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000409652.5:c.*1085G>A MANE Select ENSP00000386280.3:n.*1085G>A
ENST00000409652.4:c.*1085G>A ENSP00000386280.3:n.*1085G>A
NM_030641.3:c.*1085G>A NP_085144.1:n.*1085G>A
XM_011530392.1:c.*1085G>A XP_011528694.1:n.*1085G>A
XM_011530392.3:c.*1085G>A XP_011528694.1:n.*1085G>A
NM_030641.4:c.*1085G>A MANE Select NP_085144.1:n.*1085G>A
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