Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21239113A= , CM000674.2:g.21239113A= | GRCh38 |
| NC_000012.11:g.21392047A= , CM000674.1:g.21392047A= | GRCh37 |
| NC_000012.10:g.21283314A= | NCBI36 |
| NG_011745.1:g.112920A= , LRG_1022:g.112920A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006446.5:c.2000A= MANE Select | NP_006437.3:p.Glu667= |
| ENST00000256958.3:c.2000A= MANE Select | ENSP00000256958.2:p.Glu667= |
| NM_006446.4:c.2000A= , LRG_1022t1:c.2000A= | NP_006437.3:p.Glu667= |
| ENST00000256958.2:c.2000A= | ENSP00000256958.2:p.Glu667= |