Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10141840C= , CM000665.2:g.10141840C= | GRCh38 |
| NC_000003.11:g.10183524C= , CM000665.1:g.10183524C= | GRCh37 |
| NC_000003.10:g.10158524C= | NCBI36 |
| NG_008212.3:g.5206C= , LRG_322:g.5206C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.-8C= | ENSP00000512434.1:n.-8C= | |
| ENST00000696153.1:c.-8C= | ENSP00000512444.1:n.-8C= | |
| ENST00000256474.3:c.-8C= MANE Select | ENSP00000256474.3:n.-8C= | |
| ENST00000256474.2:c.-8C= | ENSP00000256474.2:n.-8C= | |
| ENST00000345392.2:c.-8C= | ENSP00000344757.2:n.-8C= | |
| NM_000551.3:c.-8C= , LRG_322t1:c.-8C= | NP_000542.1:n.-8C= | |
| NM_198156.2:c.-8C= | NP_937799.1:n.-8C= | |
| XM_011534078.1:c.-8C= | XP_011532380.1:n.-8C= | |
| NM_001354723.1:c.-8C= | NP_001341652.1:n.-8C= | |
| NM_000551.4:c.-8C= MANE Select | NP_000542.1:n.-8C= | |
| NM_001354723.2:c.-8C= | NP_001341652.1:n.-8C= | |
| NM_198156.3:c.-8C= | NP_937799.1:n.-8C= |