Linked Data
MyVariant Identifiers:
chr22:g.45689132C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.45293251C>A , CM000684.2:g.45293251C>A | GRCh38 |
| NC_000022.10:g.45689132C>A , CM000684.1:g.45689132C>A | GRCh37 |
| NC_000022.9:g.44067796C>A | NCBI36 |
| NG_016203.1:g.13265C>A | |
| NG_016203.2:g.13265C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216211.9:c.642C>A MANE Select | ENSP00000216211.4:p.Ile214= | |
| ENST00000216211.8:c.642C>A | ENSP00000216211.4:p.Ile214= | |
| ENST00000396082.2:c.279C>A | ENSP00000379391.2:p.Ile93= | |
| NM_001167574.1:c.279C>A | NP_001161046.1:p.Ile93= | |
| NM_006953.3:c.642C>A | NP_008884.1:p.Ile214= | |
| XM_011530364.1:c.648C>A | XP_011528666.1:p.Ile216= | |
| XM_011530365.1:c.285C>A | XP_011528667.1:p.Ile95= | |
| NM_006953.4:c.642C>A MANE Select | NP_008884.1:p.Ile214= | |
| NM_001167574.2:c.279C>A | NP_001161046.1:p.Ile93= |