Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98541879G= , CM000671.2:g.98541879G= | GRCh38 |
| NC_000009.11:g.101304161G= , CM000671.1:g.101304161G= | GRCh37 |
| NC_000009.10:g.100343982G= | NCBI36 |
| NG_016426.1:g.172319C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.624C= MANE Select | ENSP00000259455.2:p.Phe208= | |
| ENST00000637410.1:n.402C= | ||
| ENST00000259455.3:c.624C= | ENSP00000259455.2:p.Phe208= | |
| ENST00000477471.1:n.411C= | ||
| ENST00000634227.1:n.398C= | ||
| NM_005458.7:c.624C= | NP_005449.5:p.Phe208= | |
| XM_017015331.2:c.330C= | XP_016870820.1:p.Phe110= | |
| NM_005458.8:c.624C= MANE Select | NP_005449.5:p.Phe208= |