Linked Data
MyVariant Identifiers:
chr15:g.48703199A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48411002A>C , CM000677.2:g.48411002A>C | GRCh38 |
| NC_000015.9:g.48703199A>C , CM000677.1:g.48703199A>C | GRCh37 |
| NC_000015.8:g.46490491A>C | NCBI36 |
| NG_008805.2:g.239787T>G , LRG_778:g.239787T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*1412T>G | ENSP00000453958.2:n.*1412T>G | |
| ENST00000682158.1:n.1985T>G | ||
| ENST00000682170.1:n.2785T>G | ||
| ENST00000682767.1:n.1901T>G | ||
| ENST00000316623.10:c.8604T>G MANE Select | ENSP00000325527.5:p.Val2868= | |
| ENST00000316623.9:c.8604T>G | ENSP00000325527.5:p.Val2868= | |
| ENST00000559133.5:c.3973T>G | ||
| NM_000138.4:c.8604T>G , LRG_778t1:c.8604T>G | NP_000129.3:p.Val2868= | |
| NM_000138.5:c.8604T>G MANE Select | NP_000129.3:p.Val2868= |