Linked Data
MyVariant Identifiers:
chr17:g.7979022C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075704C>T , CM000679.2:g.8075704C>T | GRCh38 |
| NC_000017.10:g.7979022C>T , CM000679.1:g.7979022C>T | GRCh37 |
| NC_000017.9:g.7919747C>T | NCBI36 |
| NG_007099.1:g.17000G>A | |
| NG_007099.2:g.17013G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1545G>A MANE Select | ENSP00000497784.1:p.Glu515= | |
| ENST00000649809.1:c.609G>A | ENSP00000496845.1:p.Glu203= | |
| ENST00000319144.4:c.1545G>A | ENSP00000315167.4:p.Glu515= | |
| ENST00000577351.5:n.479+471G>A | ||
| NM_001139.2:c.1545G>A | NP_001130.1:p.Glu515= | |
| NM_001139.3:c.1545G>A MANE Select | NP_001130.1:p.Glu515= |