MyVariant.info:
GRCh38
chrY:g.12303131G>A
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.12446875 (MID)
Genomes Max Group AF
0.05114589 (AMR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12303131G>A , CM000686.2:g.12303131G>A | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651802.1:n.451-61723C>T | ||
| ENST00000651835.1:n.320-45100C>T |