Linked Data
MyVariant Identifiers:
chr17:g.41052956G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42900939G>C , CM000679.2:g.42900939G>C | GRCh38 |
| NC_000017.10:g.41052956G>C , CM000679.1:g.41052956G>C | GRCh37 |
| NC_000017.9:g.38306482G>C | NCBI36 |
| NG_011808.1:g.5142G>C , LRG_147:g.5142G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000253801.7:c.63G>C MANE Select | ENSP00000253801.1:p.Val21= | |
| ENST00000253801.6:c.63G>C | ENSP00000253801.1:p.Val21= | |
| ENST00000585489.1:c.63G>C | ENSP00000466202.1:p.Val21= | |
| ENST00000588481.1:n.128G>C | ||
| ENST00000592383.5:c.63G>C | ENSP00000465958.1:p.Val21= | |
| NM_000151.3:c.63G>C | NP_000142.2:p.Val21= | |
| NM_001270397.1:c.63G>C | NP_001257326.1:p.Val21= | |
| NM_000151.4:c.63G>C MANE Select | NP_000142.2:p.Val21= | |
| NM_001270397.2:c.63G>C | NP_001257326.1:p.Val21= |