Linked Data
MyVariant Identifiers:
chr17:g.32582407A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.34255388A>T , CM000679.2:g.34255388A>T | GRCh38 |
| NC_000017.10:g.32582407A>T , CM000679.1:g.32582407A>T | GRCh37 |
| NC_000017.9:g.29606520A>T | NCBI36 |
| NG_012123.1:g.5112A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580907.6:c.39A>T | ENSP00000462156.1:p.Ile13= | |
| ENST00000624362.2:n.104A>T | ||
| ENST00000225831.4:c.39A>T MANE Select | ENSP00000225831.4:p.Ile13= | |
| ENST00000580907.5:c.39A>T | ENSP00000462156.1:p.Ile13= | |
| ENST00000624362.1:n.171A>T | ||
| NM_002982.3:c.39A>T | NP_002973.1:p.Ile13= | |
| NM_002982.4:c.39A>T MANE Select | NP_002973.1:p.Ile13= |