HGVS | Genome Assembly |
---|---|
NC_000017.11:g.6997118T= , CM000679.2:g.6997118T= | GRCh38 |
NC_000017.10:g.6900437T= , CM000679.1:g.6900437T= | GRCh37 |
NC_000017.9:g.6841161T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251535.11:c.337+91T= (ALOX12) MANE Select | ENSP00000251535.6:n.337+91T= | |
ENST00000251535.10:c.337+91T= (ALOX12) | ENSP00000251535.6:n.337+91T= | |
ENST00000480801.1:c.46+91T= (ALOX12) | ENSP00000467033.1:n.46+91T= | |
NM_000697.2:c.337+91T= (ALOX12) | NP_000688.2:n.337+91T= | |
NR_040089.1:n.234-11578A= (ALOX12-AS1) | ||
XM_011523780.1:c.694+91T= (ALOX12) | XP_011522082.1:n.694+91T= | |
XM_011523780.2:c.694+91T= (ALOX12) | XP_011522082.1:n.694+91T= | |
NM_000697.3:c.337+91T= (ALOX12) MANE Select | NP_000688.2:n.337+91T= |