Linked Data
MyVariant Identifiers:
chr17:g.6900156T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6996837T>C , CM000679.2:g.6996837T>C | GRCh38 |
| NC_000017.10:g.6900156T>C , CM000679.1:g.6900156T>C | GRCh37 |
| NC_000017.9:g.6840880T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251535.11:c.147T>C (ALOX12) MANE Select | ENSP00000251535.6:p.Phe49= | |
| ENST00000251535.10:c.147T>C (ALOX12) | ENSP00000251535.6:p.Phe49= | |
| NM_000697.2:c.147T>C (ALOX12) | NP_000688.2:p.Phe49= | |
| NR_040089.1:n.234-11297A>G (ALOX12-AS1) | ||
| XM_011523780.1:c.504T>C (ALOX12) | XP_011522082.1:p.Phe168= | |
| XM_011523780.2:c.504T>C (ALOX12) | XP_011522082.1:p.Phe168= | |
| NM_000697.3:c.147T>C (ALOX12) MANE Select | NP_000688.2:p.Phe49= |