Linked Data
ClinVar Variation Id:
101282
ClinVar RCV Id:
RCV000087520
dbSNP Id:
rs587779571
PubMed:
PMID:10706896
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189004330G>T , CM000664.2:g.189004330G>T | GRCh38 |
| NC_000002.11:g.189869056G>T , CM000664.1:g.189869056G>T | GRCh37 |
| NC_000002.10:g.189577301G>T | NCBI36 |
| NG_007404.1:g.34958G>T , LRG_3:g.34958G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000450867.2:c.2798G>T | ENSP00000415346.2:p.Gly933Val | |
| ENST00000304636.9:c.2897G>T MANE Select | ENSP00000304408.4:p.Gly966Val | |
| ENST00000304636.7:c.2897G>T | ENSP00000304408.3:p.Gly966Val | |
| ENST00000317840.9:c.2527+1294G>T | ENSP00000315243.6:n.2527+1294G>T | |
| NM_000090.3:c.2897G>T , LRG_3t1:c.2897G>T | NP_000081.1:p.Gly966Val | |
| NM_000090.4:c.2897G>T MANE Select | NP_000081.2:p.Gly966Val |