Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7527544A= , CM000681.2:g.7527544A= | GRCh38 |
| NC_000019.9:g.7592430A= , CM000681.1:g.7592430A= | GRCh37 |
| NC_000019.8:g.7498430A= | NCBI36 |
| NG_015806.1:g.9935A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.596A= MANE Select | ENSP00000264079.5:p.Glu199= | |
| ENST00000264079.10:c.596A= | ENSP00000264079.5:p.Glu199= | |
| ENST00000394321.9:n.676A= | ||
| ENST00000598406.1:n.417A= | ||
| ENST00000601003.1:c.572-320A= | ENSP00000469074.1:n.572-320A= | |
| NM_020533.2:c.596A= | NP_065394.1:p.Glu199= | |
| NM_020533.3:c.596A= MANE Select | NP_065394.1:p.Glu199= |