Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.74789362T= , CM000669.2:g.74789362T= | GRCh38 |
| NC_000007.13:g.74203706T= , CM000669.1:g.74203706T= | GRCh37 |
| NC_000007.12:g.73841642T= | NCBI36 |
| NG_009078.2:g.20399T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289473.10:c.*202T= | ENSP00000289473.4:n.*202T= | |
| NM_000265.5:c.*202T= | NP_000256.4:n.*202T= | |
| XM_005250543.3:c.*296T= | XP_005250600.2:n.*296T= | |
| XM_011516498.1:c.*249T= | XP_011514800.1:n.*249T= | |
| XM_011516501.1:c.*202T= | XP_011514803.1:n.*202T= | |
| NM_000265.6:c.*202T= | NP_000256.4:n.*202T= |