Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186197121A= , CM000666.2:g.186197121A= | GRCh38 |
| NC_000004.11:g.187118275A= , CM000666.1:g.187118275A= | GRCh37 |
| NC_000004.10:g.187355269A= | NCBI36 |
| NG_007965.1:g.10602A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.595A= MANE Select | ENSP00000368079.4:p.Ile199= | |
| ENST00000378802.4:c.595A= | ENSP00000368079.4:p.Ile199= | |
| ENST00000507209.5:n.1034A= | ||
| NM_207352.3:c.595A= | NP_997235.3:p.Ile199= | |
| XM_005262935.2:c.595A= | XP_005262992.1:p.Ile199= | |
| XM_006714184.2:c.199A= | XP_006714247.1:p.Ile67= | |
| XM_005262935.4:c.595A= | XP_005262992.1:p.Ile199= | |
| XM_017008037.1:c.199A= | XP_016863526.1:p.Ile67= | |
| NM_207352.4:c.595A= MANE Select | NP_997235.3:p.Ile199= |