Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.40867155G>C , CM000679.2:g.40867155G>C | GRCh38 |
| NC_000017.10:g.39023407G>C , CM000679.1:g.39023407G>C | GRCh37 |
| NC_000017.9:g.36276933G>C | NCBI36 |
| NG_008077.1:g.5056C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000251643.5:c.32C>G MANE Select | ENSP00000251643.4:p.Ser11Ter | |
| ENST00000647902.1:c.32C>G | ENSP00000497770.1:p.Ser11Ter | |
| ENST00000251643.4:c.32C>G | ENSP00000251643.4:p.Ser11Ter | |
| NM_000223.3:c.32C>G | NP_000214.1:p.Ser11Ter | |
| XR_934754.1:n.1500+16295G>C | ||
| XR_934754.2:n.2008+16295G>C | ||
| NM_000223.4:c.32C>G MANE Select | NP_000214.1:p.Ser11Ter |