Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176119524C= , CM000664.2:g.176119524C= | GRCh38 |
| NC_000002.11:g.176984252C= , CM000664.1:g.176984252C= | GRCh37 |
| NC_000002.10:g.176692498C= | NCBI36 |
| NG_008133.2:g.12761C= , LRG_246:g.12761C= | |
| NG_009225.1:g.1840C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249501.5:c.*293C= MANE Select | ENSP00000249501.4:n.*293C= | |
| ENST00000249501.4:c.*293C= | ENSP00000249501.4:n.*293C= | |
| NM_002148.3:c.*293C= , LRG_246t1:c.*293C= | NP_002139.2:n.*293C= | |
| NM_002148.4:c.*293C= MANE Select | NP_002139.2:n.*293C= |