Revel Score:
ENST00000222304 (MANE Select)
0.329
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35284953C>G , CM000681.2:g.35284953C>G | GRCh38 |
| NC_000019.9:g.35775856C>G , CM000681.1:g.35775856C>G | GRCh37 |
| NC_000019.8:g.40467696C>G | NCBI36 |
| NG_011563.1:g.7447C>G | |
| NG_011563.2:g.7447C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222304.5:c.166C>G MANE Select | ENSP00000222304.2:p.Arg56Gly | |
| ENST00000222304.3:c.166C>G | ENSP00000222304.2:p.Arg56Gly | |
| ENST00000593580.1:n.2437C>G | ||
| ENST00000598398.5:c.166C>G | ENSP00000471894.1:p.Arg56Gly | |
| NM_021175.2:c.166C>G | NP_066998.1:p.Arg56Gly | |
| NM_021175.3:c.166C>G | NP_066998.1:p.Arg56Gly | |
| NM_021175.4:c.166C>G MANE Select | NP_066998.1:p.Arg56Gly |