HGVS | Genome Assembly |
---|---|
NC_000017.11:g.6996875T>G , CM000679.2:g.6996875T>G | GRCh38 |
NC_000017.10:g.6900194T>G , CM000679.1:g.6900194T>G | GRCh37 |
NC_000017.9:g.6840918T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251535.11:c.185T>G (ALOX12) MANE Select | ENSP00000251535.6:p.Phe62Cys | |
ENST00000251535.10:c.185T>G (ALOX12) | ENSP00000251535.6:p.Phe62Cys | |
NM_000697.2:c.185T>G (ALOX12) | NP_000688.2:p.Phe62Cys | |
NR_040089.1:n.234-11335A>C (ALOX12-AS1) | ||
XM_011523780.1:c.542T>G (ALOX12) | XP_011522082.1:p.Phe181Cys | |
XM_011523780.2:c.542T>G (ALOX12) | XP_011522082.1:p.Phe181Cys | |
NM_000697.3:c.185T>G (ALOX12) MANE Select | NP_000688.2:p.Phe62Cys |