Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745474T= , CM000665.2:g.8745474T= | GRCh38 |
| NC_000003.11:g.8787160T= , CM000665.1:g.8787160T= | GRCh37 |
| NC_000003.10:g.8762160T= | NCBI36 |
| NG_008797.2:g.16665T= , LRG_329:g.16665T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343849.3:c.115-52T= MANE Select | ENSP00000341940.2:n.115-52T= | |
| ENST00000343849.2:c.115-52T= | ENSP00000341940.2:n.115-52T= | |
| ENST00000397368.2:c.115-52T= | ENSP00000380525.2:n.115-52T= | |
| ENST00000472766.1:n.155+11484T= | ||
| NM_001234.4:c.115-52T= | NP_001225.1:n.115-52T= | |
| NM_033337.2:c.115-52T= , LRG_329t1:c.115-52T= | NP_203123.1:n.115-52T= | |
| NM_001234.5:c.115-52T= | NP_001225.1:n.115-52T= | |
| NM_033337.3:c.115-52T= MANE Select | NP_203123.1:n.115-52T= |