Linked Data
MyVariant Identifiers:
chr17:g.32582398G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.34255379G>T , CM000679.2:g.34255379G>T | GRCh38 |
| NC_000017.10:g.32582398G>T , CM000679.1:g.32582398G>T | GRCh37 |
| NC_000017.9:g.29606511G>T | NCBI36 |
| NG_012123.1:g.5103G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580907.6:c.30G>T | ENSP00000462156.1:p.Leu10= | |
| ENST00000624362.2:n.95G>T | ||
| ENST00000225831.4:c.30G>T MANE Select | ENSP00000225831.4:p.Leu10= | |
| ENST00000580907.5:c.30G>T | ENSP00000462156.1:p.Leu10= | |
| ENST00000624362.1:n.162G>T | ||
| NM_002982.3:c.30G>T | NP_002973.1:p.Leu10= | |
| NM_002982.4:c.30G>T MANE Select | NP_002973.1:p.Leu10= |