Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.106463593A= , CM000674.2:g.106463593A= | GRCh38 |
| NC_000012.11:g.106857371A= , CM000674.1:g.106857371A= | GRCh37 |
| NC_000012.10:g.105381501A= | NCBI36 |
| NG_031837.1:g.110936A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_018082.6:c.2686A= MANE Select | NP_060552.4:p.Lys896= |
| ENST00000228347.9:c.2686A= MANE Select | ENSP00000228347.4:p.Lys896= |
| NM_001160708.1:c.2512A= | NP_001154180.1:p.Lys838= |
| NM_001160708.2:c.2512A= | NP_001154180.1:p.Lys838= |
| NM_018082.5:c.2686A= | NP_060552.4:p.Lys896= |
| ENST00000228347.8:c.2686A= | ENSP00000228347.4:p.Lys896= |
| ENST00000539066.5:c.2512A= | ENSP00000445721.1:p.Lys838= |
| XM_017019621.2:c.2686A= | XP_016875110.1:p.Lys896= |