Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176093682T= , CM000664.2:g.176093682T= | GRCh38 |
| NC_000002.11:g.176958410T= , CM000664.1:g.176958410T= | GRCh37 |
| NC_000002.10:g.176666656T= | NCBI36 |
| NG_008137.1:g.5879T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392539.4:c.781+11T= MANE Select | ENSP00000376322.3:n.781+11T= | |
| ENST00000392539.3:c.781+11T= | ENSP00000376322.3:n.781+11T= | |
| NM_000523.3:c.781+11T= | NP_000514.2:n.781+11T= | |
| XM_011511068.1:c.725-798T= | XP_011509370.1:n.725-798T= | |
| XM_011511068.2:c.725-798T= | XP_011509370.1:n.725-798T= | |
| NM_000523.4:c.781+11T= MANE Select | NP_000514.2:n.781+11T= |