Linked Data
MyVariant Identifiers:
chr17:g.6904932C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7001613C>T , CM000679.2:g.7001613C>T | GRCh38 |
| NC_000017.10:g.6904932C>T , CM000679.1:g.6904932C>T | GRCh37 |
| NC_000017.9:g.6845656C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251535.11:c.963C>T (ALOX12) MANE Select | ENSP00000251535.6:p.Pro321= | |
| ENST00000251535.10:c.963C>T (ALOX12) | ENSP00000251535.6:p.Pro321= | |
| NM_000697.2:c.963C>T (ALOX12) | NP_000688.2:p.Pro321= | |
| NR_040089.1:n.233+8183G>A (ALOX12-AS1) | ||
| XM_011523780.1:c.1113C>T (ALOX12) | XP_011522082.1:p.Pro371= | |
| XM_011523780.2:c.1113C>T (ALOX12) | XP_011522082.1:p.Pro371= | |
| NM_000697.3:c.963C>T (ALOX12) MANE Select | NP_000688.2:p.Pro321= |