Linked Data
MyVariant Identifiers:
chr17:g.42429154A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44351786A>G , CM000679.2:g.44351786A>G | GRCh38 |
| NC_000017.10:g.42429154A>G , CM000679.1:g.42429154A>G | GRCh37 |
| NC_000017.9:g.39784680A>G | NCBI36 |
| NG_007886.1:g.11664A>G , LRG_661:g.11664A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000053867.8:c.1170A>G MANE Select | ENSP00000053867.2:p.Pro390= | |
| ENST00000639447.1:c.1136+34A>G | ENSP00000492014.1:n.1136+34A>G | |
| ENST00000053867.7:c.1170A>G | ENSP00000053867.2:p.Pro390= | |
| ENST00000586443.1:c.611A>G | ||
| ENST00000589265.5:c.699A>G | ENSP00000467616.1:p.Pro233= | |
| ENST00000589923.1:n.428A>G | ||
| NM_002087.3:c.1170A>G | NP_002078.1:p.Pro390= | |
| XM_005257253.1:c.1170A>G | XP_005257310.1:p.Pro390= | |
| XM_024450730.1:c.1170A>G | XP_024306498.1:p.Pro390= | |
| NM_002087.4:c.1170A>G MANE Select | NP_002078.1:p.Pro390= |