Linked Data
MyVariant Identifiers:
chr17:g.41063416G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911399G>C , CM000679.2:g.42911399G>C | GRCh38 |
| NC_000017.10:g.41063416G>C , CM000679.1:g.41063416G>C | GRCh37 |
| NC_000017.9:g.38316942G>C | NCBI36 |
| NG_011808.1:g.15602G>C , LRG_147:g.15602G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.1047G>C MANE Select | ENSP00000253801.1:p.Leu349= | |
| ENST00000253801.6:c.1047G>C | ENSP00000253801.1:p.Leu349= | |
| ENST00000585489.1:c.*439G>C | ENSP00000466202.1:n.*439G>C | |
| NM_000151.3:c.1047G>C | NP_000142.2:p.Leu349= | |
| NM_001270397.1:c.*439G>C | NP_001257326.1:n.*439G>C | |
| NM_000151.4:c.1047G>C MANE Select | NP_000142.2:p.Leu349= | |
| NM_001270397.2:c.*439G>C | NP_001257326.1:n.*439G>C |