Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10141784C= , CM000665.2:g.10141784C= | GRCh38 |
| NC_000003.11:g.10183468C= , CM000665.1:g.10183468C= | GRCh37 |
| NC_000003.10:g.10158468C= | NCBI36 |
| NG_008212.3:g.5150C= , LRG_322:g.5150C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696153.1:c.-64C= | ENSP00000512444.1:n.-64C= | |
| ENST00000256474.3:c.-64C= MANE Select | ENSP00000256474.3:n.-64C= | |
| ENST00000256474.2:c.-64C= | ENSP00000256474.2:n.-64C= | |
| NM_000551.3:c.-64C= , LRG_322t1:c.-64C= | NP_000542.1:n.-64C= | |
| NM_198156.2:c.-64C= | NP_937799.1:n.-64C= | |
| XM_011534078.1:c.-64C= | XP_011532380.1:n.-64C= | |
| NM_001354723.1:c.-64C= | NP_001341652.1:n.-64C= | |
| NM_000551.4:c.-64C= MANE Select | NP_000542.1:n.-64C= | |
| NM_001354723.2:c.-64C= | NP_001341652.1:n.-64C= | |
| NM_198156.3:c.-64C= | NP_937799.1:n.-64C= |