Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49128754G>A , CM000665.2:g.49128754G>A | GRCh38 |
| NC_000003.11:g.49166187G>A , CM000665.1:g.49166187G>A | GRCh37 |
| NC_000003.10:g.49141191G>A | NCBI36 |
| NG_008094.1:g.9413C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002292.4:c.1797C>T MANE Select | NP_002283.3:p.Phe599= |
| ENST00000305544.9:c.1797C>T MANE Select | ENSP00000307156.4:p.Phe599= |
| NM_002292.3:c.1797C>T | NP_002283.3:p.Phe599= |
| ENST00000305544.8:c.1797C>T | ENSP00000307156.4:p.Phe599= |
| ENST00000418109.5:c.1797C>T | ENSP00000388325.1:p.Phe599= |
| ENST00000483321.1:n.227C>T | |
| XM_005265127.3:c.1797C>T | XP_005265184.1:p.Phe599= |
| XM_005265127.4:c.1797C>T | XP_005265184.1:p.Phe599= |