Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189004177T= , CM000664.2:g.189004177T= | GRCh38 |
| NC_000002.11:g.189868903T= , CM000664.1:g.189868903T= | GRCh37 |
| NC_000002.10:g.189577148T= | NCBI36 |
| NG_007404.1:g.34805T= , LRG_3:g.34805T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.2724+34T= | ENSP00000415346.2:n.2724+34T= | |
| ENST00000304636.9:c.2823+34T= MANE Select | ENSP00000304408.4:n.2823+34T= | |
| ENST00000304636.7:c.2823+34T= | ENSP00000304408.3:n.2823+34T= | |
| ENST00000317840.9:c.2527+1141T= | ENSP00000315243.6:n.2527+1141T= | |
| NM_000090.3:c.2823+34T= , LRG_3t1:c.2823+34T= | NP_000081.1:n.2823+34T= | |
| NM_000090.4:c.2823+34T= MANE Select | NP_000081.2:n.2823+34T= |