Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31860458A= , CM000668.2:g.31860458A= | GRCh38 |
| NC_000006.11:g.31828235A= , CM000668.1:g.31828235A= | GRCh37 |
| NC_000006.10:g.31936214A= | NCBI36 |
| NG_008201.1:g.7475T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000434.4:c.779T= MANE Select | NP_000425.1:p.Phe260= |
| ENST00000375631.5:c.779T= MANE Select | ENSP00000364782.4:p.Phe260= |
| NM_000434.3:c.779T= | NP_000425.1:p.Phe260= |
| ENST00000375631.4:c.779T= | ENSP00000364782.4:p.Phe260= |
| ENST00000480384.1:n.808T= | |
| ENST00000491768.5:c.779T= | ENSP00000433127.1:p.Phe260= |
| ENST00000495807.1:n.1913T= | |
| ENST00000677054.1:n.2022T= | |
| ENST00000677512.1:n.887T= | |
| ENST00000678869.1:n.1453T= |