Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571417A= , CM000663.2:g.154571417A= | GRCh38 |
| NC_000001.10:g.154543893A= , CM000663.1:g.154543893A= | GRCh37 |
| NC_000001.9:g.152810517A= | NCBI36 |
| NG_008027.1:g.8637A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.594A= MANE Select | ENSP00000357461.3:p.Thr198= | |
| ENST00000636034.1:c.594A= | ENSP00000489703.1:p.Thr198= | |
| ENST00000637900.1:c.600A= | ENSP00000490474.1:p.Thr200= | |
| ENST00000368476.3:c.594A= | ENSP00000357461.3:p.Thr198= | |
| NM_000748.2:c.594A= | NP_000739.1:p.Thr198= | |
| XM_017000180.2:c.84A= | XP_016855669.1:p.Thr28= | |
| XR_001736952.2:n.846A= | ||
| NM_000748.3:c.594A= MANE Select | NP_000739.1:p.Thr198= |