Linked Data
MyVariant Identifiers:
chr17:g.16875342G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.16972028G>A , CM000679.2:g.16972028G>A | GRCh38 |
| NC_000017.10:g.16875342G>A , CM000679.1:g.16875342G>A | GRCh37 |
| NC_000017.9:g.16816067G>A | NCBI36 |
| NG_007281.1:g.5061C>T , LRG_120:g.5061C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261652.7:c.48C>T MANE Select | ENSP00000261652.2:p.Asp16= | |
| ENST00000261652.6:c.48C>T | ENSP00000261652.2:p.Asp16= | |
| ENST00000579315.5:c.48C>T | ENSP00000464069.1:p.Asp16= | |
| ENST00000581616.2:n.51C>T | ||
| ENST00000582931.5:n.90C>T | ||
| ENST00000583789.1:c.48C>T | ENSP00000462952.1:p.Asp16= | |
| ENST00000584950.5:c.48C>T | ENSP00000463582.1:p.Asp16= | |
| NM_012452.2:c.48C>T , LRG_120t1:c.48C>T | NP_036584.1:p.Asp16= | |
| NM_012452.3:c.48C>T MANE Select | NP_036584.1:p.Asp16= |