Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1213554T= , CM000667.2:g.1213554T= | GRCh38 |
| NC_000005.9:g.1213669T= , CM000667.1:g.1213669T= | GRCh37 |
| NC_000005.8:g.1266669T= | NCBI36 |
| NG_008282.1:g.16960T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304460.11:c.755T= MANE Select | ENSP00000305302.10:p.Val252= | |
| ENST00000304460.10:c.755T= | ENSP00000305302.10:p.Val252= | |
| ENST00000515652.5:c.663T= | ENSP00000425701.1:p.Arg221= | |
| NM_001003841.2:c.755T= | NP_001003841.1:p.Val252= | |
| NM_001003841.3:c.755T= MANE Select | NP_001003841.1:p.Val252= |