Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624247A>G , CM000679.2:g.41624247A>G | GRCh38 |
| NC_000017.10:g.39780499A>G , CM000679.1:g.39780499A>G | GRCh37 |
| NC_000017.9:g.37034025A>G | NCBI36 |
| NG_008625.1:g.5384T>C | |
| NG_009090.2:g.167466T>C , LRG_401:g.167466T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.263T>C MANE Select | ENSP00000308452.8:p.Met88Thr | |
| ENST00000311208.12:c.263T>C | ENSP00000308452.8:p.Met88Thr | |
| ENST00000463128.5:c.-312-41T>C | ENSP00000468672.1:n.-312-41T>C | |
| ENST00000491673.1:n.329T>C | ||
| ENST00000493253.5:n.50T>C | ||
| ENST00000540235.5:c.58T>C | ENSP00000441751.2:p.Cys20Arg | |
| ENST00000577817.3:c.218T>C | ENSP00000467418.1:p.Met73Thr | |
| NM_000422.2:c.263T>C | NP_000413.1:p.Met88Thr | |
| NM_000422.3:c.263T>C MANE Select | NP_000413.1:p.Met88Thr |