Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18785007A>G , CM000681.2:g.18785007A>G | GRCh38 |
| NC_000019.9:g.18895817A>G , CM000681.1:g.18895817A>G | GRCh37 |
| NC_000019.8:g.18756817A>G | NCBI36 |
| NG_007070.1:g.11298T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000095.3:c.1803T>C MANE Select | NP_000086.2:p.Phe601= |
| ENST00000222271.7:c.1803T>C MANE Select | ENSP00000222271.2:p.Phe601= |
| NM_000095.2:c.1803T>C | NP_000086.2:p.Phe601= |
| ENST00000222271.6:c.1803T>C | ENSP00000222271.2:p.Phe601= |
| ENST00000425807.1:c.1644T>C | ENSP00000403792.1:p.Phe548= |
| ENST00000542601.6:c.1704T>C | ENSP00000439156.2:p.Phe568= |