Linked Data
dbSNP Id:
rs966014348
gnomAD v2:
17-6900142-CAGG-C
gnomAD v3:
17-6996823-CAGG-C
gnomAD v4:
17-6996823-CAGG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6996832_6996834del , CM000679.2:g.6996832_6996834del | GRCh38 |
| NC_000017.10:g.6900151_6900153del , CM000679.1:g.6900151_6900153del | GRCh37 |
| NC_000017.9:g.6840875_6840877del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251535.11:c.142_144del (ALOX12) | ||
| ENST00000251535.10:c.142_144del (ALOX12) | ||
| NM_000697.2:c.142_144del (ALOX12) | ||
| NR_040089.1:n.234-11286_234-11284del (ALOX12-AS1) | ||
| XM_011523780.1:c.499_501del (ALOX12) | ||
| XM_011523780.2:c.499_501del (ALOX12) | ||
| NM_000697.3:c.142_144del (ALOX12) |