Linked Data
MyVariant Identifiers:
chr17:g.62049828G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63972468G>T , CM000679.2:g.63972468G>T | GRCh38 |
| NC_000017.10:g.62049828G>T , CM000679.1:g.62049828G>T | GRCh37 |
| NC_000017.9:g.59403560G>T | NCBI36 |
| NG_011699.1:g.5451C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.276C>A MANE Select | ENSP00000396320.1:p.Thr92= | |
| ENST00000578147.5:c.276C>A | ENSP00000463963.1:p.Thr92= | |
| NM_000334.4:c.276C>A MANE Select | NP_000325.4:p.Thr92= | |
| XM_005257566.3:c.276C>A | XP_005257623.1:p.Thr92= |