Linked Data
MyVariant Identifiers:
chr17:g.7979016G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075698G>T , CM000679.2:g.8075698G>T | GRCh38 |
| NC_000017.10:g.7979016G>T , CM000679.1:g.7979016G>T | GRCh37 |
| NC_000017.9:g.7919741G>T | NCBI36 |
| NG_007099.1:g.17006C>A | |
| NG_007099.2:g.17019C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647874.1:c.1551C>A MANE Select | ENSP00000497784.1:p.Ile517= | |
| ENST00000649809.1:c.615C>A | ENSP00000496845.1:p.Ile205= | |
| ENST00000319144.4:c.1551C>A | ENSP00000315167.4:p.Ile517= | |
| ENST00000577351.5:n.479+477C>A | ||
| NM_001139.2:c.1551C>A | NP_001130.1:p.Ile517= | |
| NM_001139.3:c.1551C>A MANE Select | NP_001130.1:p.Ile517= |