Revel Score:
ENST00000263388 (MANE Select)
0.171
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15160960G>C , CM000681.2:g.15160960G>C | GRCh38 |
| NC_000019.9:g.15271771G>C , CM000681.1:g.15271771G>C | GRCh37 |
| NC_000019.8:g.15132771G>C | NCBI36 |
| NG_009819.1:g.45022C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263388.7:c.6668C>G MANE Select | ENSP00000263388.1:p.Ala2223Gly | |
| ENST00000263388.6:c.6668C>G | ENSP00000263388.1:p.Ala2223Gly | |
| NM_000435.2:c.6668C>G | NP_000426.2:p.Ala2223Gly | |
| XM_005259924.3:c.6512C>G | XP_005259981.1:p.Ala2171Gly | |
| XM_005259924.4:c.6512C>G | XP_005259981.1:p.Ala2171Gly | |
| NM_000435.3:c.6668C>G MANE Select | NP_000426.2:p.Ala2223Gly |