Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.10622754T= , CM000670.2:g.10622754T= | GRCh38 |
| NC_000008.10:g.10480264T= , CM000670.1:g.10480264T= | GRCh37 |
| NC_000008.9:g.10517674T= | NCBI36 |
| NG_028035.1:g.37354A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382483.4:c.448A= MANE Select | ENSP00000371923.3:p.Thr150= | |
| ENST00000329335.3:n.698A= | ||
| ENST00000382483.3:c.448A= | ENSP00000371923.3:p.Thr150= | |
| NM_178857.5:c.448A= | NP_849188.4:p.Thr150= | |
| NM_178857.6:c.448A= MANE Select | NP_849188.4:p.Thr150= |