Linked Data
MyVariant Identifiers:
chr11:g.116703567T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116832851T>G , CM000673.2:g.116832851T>G | GRCh38 |
| NC_000011.9:g.116703567T>G , CM000673.1:g.116703567T>G | GRCh37 |
| NC_000011.8:g.116208777T>G | NCBI36 |
| NG_008949.1:g.7944T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227667.8:c.267T>G MANE Select | ENSP00000227667.2:p.Pro89= | |
| ENST00000227667.7:c.267T>G | ENSP00000227667.2:p.Pro89= | |
| ENST00000375345.3:c.321T>G | ENSP00000364494.1:p.Pro107= | |
| ENST00000630701.1:c.321T>G | ENSP00000486182.1:p.Pro107= | |
| NM_000040.1:c.267T>G | NP_000031.1:p.Pro89= | |
| NM_000040.2:c.267T>G | NP_000031.1:p.Pro89= | |
| NM_000040.3:c.267T>G MANE Select | NP_000031.1:p.Pro89= |