Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6145478G= , CM000668.2:g.6145478G= | GRCh38 |
| NC_000006.11:g.6145711G= , CM000668.1:g.6145711G= | GRCh37 |
| NC_000006.10:g.6090710G= | NCBI36 |
| NG_008107.1:g.180214C= , LRG_549:g.180214C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.*141C= MANE Select | ENSP00000264870.3:n.*141C= | |
| ENST00000264870.7:c.*141C= | ENSP00000264870.3:n.*141C= | |
| NM_000129.3:c.*141C= , LRG_549t1:c.*141C= | NP_000120.2:n.*141C= | |
| XM_006715010.2:c.*141C= | XP_006715073.1:n.*141C= | |
| XM_011514342.1:c.*141C= | XP_011512644.1:n.*141C= | |
| NM_000129.4:c.*141C= MANE Select | NP_000120.2:n.*141C= |