Linked Data
MyVariant Identifiers:
chr17:g.32582399C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.34255380C>T , CM000679.2:g.34255380C>T | GRCh38 |
| NC_000017.10:g.32582399C>T , CM000679.1:g.32582399C>T | GRCh37 |
| NC_000017.9:g.29606512C>T | NCBI36 |
| NG_012123.1:g.5104C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580907.6:c.31C>T | ENSP00000462156.1:p.Leu11= | |
| ENST00000624362.2:n.96C>T | ||
| ENST00000225831.4:c.31C>T MANE Select | ENSP00000225831.4:p.Leu11= | |
| ENST00000580907.5:c.31C>T | ENSP00000462156.1:p.Leu11= | |
| ENST00000624362.1:n.163C>T | ||
| NM_002982.3:c.31C>T | NP_002973.1:p.Leu11= | |
| NM_002982.4:c.31C>T MANE Select | NP_002973.1:p.Leu11= |