Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745534T= , CM000665.2:g.8745534T= | GRCh38 |
| NC_000003.11:g.8787220T= , CM000665.1:g.8787220T= | GRCh37 |
| NC_000003.10:g.8762220T= | NCBI36 |
| NG_008797.2:g.16725T= , LRG_329:g.16725T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343849.3:c.123T= MANE Select | ENSP00000341940.2:p.Phe41= | |
| ENST00000343849.2:c.123T= | ENSP00000341940.2:p.Phe41= | |
| ENST00000397368.2:c.123T= | ENSP00000380525.2:p.Phe41= | |
| ENST00000472766.1:n.155+11544T= | ||
| NM_001234.4:c.123T= | NP_001225.1:p.Phe41= | |
| NM_033337.2:c.123T= , LRG_329t1:c.123T= | NP_203123.1:p.Phe41= | |
| NM_001234.5:c.123T= | NP_001225.1:p.Phe41= | |
| NM_033337.3:c.123T= MANE Select | NP_203123.1:p.Phe41= |