Revel Score:
ENST00000337818
0.829
ENST00000216181 (MANE Select)
0.829
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36305975C>T , CM000684.2:g.36305975C>T | GRCh38 |
| NC_000022.10:g.36702021C>T , CM000684.1:g.36702021C>T | GRCh37 |
| NC_000022.9:g.35031967C>T | NCBI36 |
| NG_011884.2:g.87044G>A , LRG_567:g.87044G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685801.1:c.2177G>A | ENSP00000510688.1:p.Arg726His | |
| ENST00000687922.1:n.450G>A | ||
| ENST00000691109.1:n.2409G>A | ||
| ENST00000216181.11:c.2114G>A MANE Select | ENSP00000216181.6:p.Arg705His | |
| ENST00000216181.9:c.2114G>A | ENSP00000216181.5:p.Arg705His | |
| NM_002473.5:c.2114G>A , LRG_567t1:c.2114G>A | NP_002464.1:p.Arg705His | |
| XM_011530197.1:c.2114G>A | XP_011528499.1:p.Arg705His | |
| XM_011530197.2:c.2114G>A | XP_011528499.1:p.Arg705His | |
| XM_017028803.1:c.2114G>A | XP_016884292.1:p.Arg705His | |
| XM_017028804.1:c.2114G>A | XP_016884293.1:p.Arg705His | |
| XM_017028805.1:c.2114G>A | XP_016884294.1:p.Arg705His | |
| XM_017028806.1:c.2114G>A | XP_016884295.1:p.Arg705His | |
| NM_002473.6:c.2114G>A MANE Select | NP_002464.1:p.Arg705His |