Linked Data
MyVariant Identifiers:
chr13:g.28498406T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924269T>G , CM000675.2:g.27924269T>G | GRCh38 |
| NC_000013.10:g.28498406T>G , CM000675.1:g.28498406T>G | GRCh37 |
| NC_000013.9:g.27396406T>G | NCBI36 |
| NG_008183.1:g.9239T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.420T>G MANE Select | ENSP00000370421.4:p.Ala140= | |
| ENST00000381033.4:c.420T>G | ENSP00000370421.4:p.Ala140= | |
| NM_000209.3:c.420T>G | NP_000200.1:p.Ala140= | |
| XR_941578.1:n.3547T>G | ||
| XR_941579.1:n.2146T>G | ||
| XR_941580.1:n.1062T>G | ||
| XR_941578.2:n.3559T>G | ||
| XR_941580.2:n.1074T>G | ||
| NM_000209.4:c.420T>G MANE Select | NP_000200.1:p.Ala140= |