Linked Data
dbSNP Id:
rs1370769509
gnomAD v2:
17-6899909-GGGACC-G
gnomAD v3:
17-6996590-GGGACC-G
gnomAD v4:
17-6996590-GGGACC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6996591_6996595del , CM000679.2:g.6996591_6996595del | GRCh38 |
| NC_000017.10:g.6899910_6899914del , CM000679.1:g.6899910_6899914del | GRCh37 |
| NC_000017.9:g.6840634_6840638del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251535.11:c.136-235_136-231del (ALOX12) MANE Select | ENSP00000251535.6:n.136-235_136-231del | |
| ENST00000251535.10:c.136-235_136-231del (ALOX12) | ENSP00000251535.6:n.136-235_136-231del | |
| NM_000697.2:c.136-235_136-231del (ALOX12) | NP_000688.2:n.136-235_136-231del | |
| NR_040089.1:n.234-11055_234-11051del (ALOX12-AS1) | ||
| XM_011523780.1:c.493-235_493-231del (ALOX12) | XP_011522082.1:n.493-235_493-231del | |
| XM_011523780.2:c.493-235_493-231del (ALOX12) | XP_011522082.1:n.493-235_493-231del | |
| NM_000697.3:c.136-235_136-231del (ALOX12) MANE Select | NP_000688.2:n.136-235_136-231del |