Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624284C= , CM000679.2:g.41624284C= | GRCh38 |
| NC_000017.10:g.39780536C= , CM000679.1:g.39780536C= | GRCh37 |
| NC_000017.9:g.37034062C= | NCBI36 |
| NG_008625.1:g.5347G= | |
| NG_009090.2:g.167429G= , LRG_401:g.167429G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.226G= MANE Select | ENSP00000308452.8:p.Val76= | |
| ENST00000311208.12:c.226G= | ENSP00000308452.8:p.Val76= | |
| ENST00000463128.5:c.-312-78G= | ENSP00000468672.1:n.-312-78G= | |
| ENST00000491673.1:n.292G= | ||
| ENST00000493253.5:n.13G= | ||
| ENST00000540235.5:c.21G= | ENSP00000441751.2:p.Val7= | |
| ENST00000577817.3:c.181G= | ENSP00000467418.1:p.Val61= | |
| NM_000422.2:c.226G= | NP_000413.1:p.Val76= | |
| NM_000422.3:c.226G= MANE Select | NP_000413.1:p.Val76= |