Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49950952T>G , CM000674.2:g.49950952T>G | GRCh38 |
| NC_000012.11:g.50344735T>G , CM000674.1:g.50344735T>G | GRCh37 |
| NC_000012.10:g.48631002T>G | NCBI36 |
| NG_008913.1:g.5212T>G , LRG_717:g.5212T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000199280.4:c.122T>G MANE Select | ENSP00000199280.3:p.Val41Gly | |
| ENST00000199280.3:c.122T>G | ENSP00000199280.3:p.Val41Gly | |
| ENST00000550862.1:c.122T>G | ENSP00000450022.1:p.Val41Gly | |
| ENST00000551526.5:c.122T>G | ENSP00000447148.1:p.Val41Gly | |
| NM_000486.5:c.122T>G , LRG_717t1:c.122T>G | NP_000477.1:p.Val41Gly | |
| NM_000486.6:c.122T>G MANE Select | NP_000477.1:p.Val41Gly |