Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19954174C= , CM000670.2:g.19954174C= | GRCh38 |
| NC_000008.10:g.19811685C= , CM000670.1:g.19811685C= | GRCh37 |
| NC_000008.9:g.19855965C= | NCBI36 |
| NG_008855.1:g.20104C= | |
| NG_008855.2:g.57458C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.596C= MANE Select | ENSP00000497642.1:p.Ser199= | |
| ENST00000311322.8:c.596C= | ENSP00000309757.6:p.Ser199= | |
| NM_000237.2:c.596C= | NP_000228.1:p.Ser199= | |
| NM_000237.3:c.596C= MANE Select | NP_000228.1:p.Ser199= |