Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624178T= , CM000679.2:g.41624178T= | GRCh38 |
| NC_000017.10:g.39780430T= , CM000679.1:g.39780430T= | GRCh37 |
| NC_000017.9:g.37033956T= | NCBI36 |
| NG_008625.1:g.5453A= | |
| NG_009090.2:g.167535A= , LRG_401:g.167535A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.332A= MANE Select | ENSP00000308452.8:p.Glu111= | |
| ENST00000311208.12:c.332A= | ENSP00000308452.8:p.Glu111= | |
| ENST00000463128.5:c.-284A= | ENSP00000468672.1:n.-284A= | |
| ENST00000491673.1:n.398A= | ||
| ENST00000493253.5:n.119A= | ||
| ENST00000540235.5:c.83A= | ENSP00000441751.2:p.Glu28= | |
| ENST00000577817.3:c.287A= | ENSP00000467418.1:p.Glu96= | |
| NM_000422.2:c.332A= | NP_000413.1:p.Glu111= | |
| NM_000422.3:c.332A= MANE Select | NP_000413.1:p.Glu111= |