Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81577875T= , CM000665.2:g.81577875T= | GRCh38 |
| NC_000003.11:g.81627026T= , CM000665.1:g.81627026T= | GRCh37 |
| NC_000003.10:g.81709716T= | NCBI36 |
| NG_011810.1:g.188926A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.1618+50A= MANE Select | ENSP00000410833.2:n.1618+50A= | |
| ENST00000429644.6:c.1618+50A= | ENSP00000410833.2:n.1618+50A= | |
| ENST00000484687.1:n.19+50A= | ||
| ENST00000489715.1:c.1495+50A= | ENSP00000419638.1:n.1495+50A= | |
| NM_000158.3:c.1618+50A= | NP_000149.3:n.1618+50A= | |
| NM_000158.4:c.1618+50A= MANE Select | NP_000149.4:n.1618+50A= |