Revel Score:
ENST00000316300 (MANE Select)
0.352
ENST00000447678
0.352
gnomAD v2:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160650438G>C , CM000668.2:g.160650438G>C | GRCh38 |
| NC_000006.11:g.161071470G>C , CM000668.1:g.161071470G>C | GRCh37 |
| NC_000006.10:g.160991460G>C | NCBI36 |
| NG_016147.1:g.20938C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316300.10:c.109C>G MANE Select | ENSP00000321334.6:p.Arg37Gly | |
| ENST00000316300.9:c.109C>G | ENSP00000321334.5:p.Arg37Gly | |
| NM_005577.2:c.109C>G | NP_005568.2:p.Arg37Gly | |
| NM_005577.3:c.109C>G | NP_005568.2:p.Arg37Gly | |
| NM_005577.4:c.109C>G MANE Select | NP_005568.2:p.Arg37Gly |