Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49664550G= , CM000665.2:g.49664550G= | GRCh38 |
| NC_000003.11:g.49701983G= , CM000665.1:g.49701983G= | GRCh37 |
| NC_000003.10:g.49676987G= | NCBI36 |
| NG_015892.1:g.115062G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003458.4:c.11736G= MANE Select | NP_003449.2:p.Thr3912= |
| ENST00000296452.5:c.11736G= MANE Select | ENSP00000296452.4:p.Thr3912= |
| NM_003458.3:c.11736G= | NP_003449.2:p.Thr3912= |
| ENST00000296452.4:c.11736G= | ENSP00000296452.4:p.Thr3912= |