Linked Data
ClinVar Variation Id:
101430
ClinVar RCV Id:
RCV000087668
dbSNP Id:
rs587779673
PubMed:
PMID:24922459
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188992888G>A , CM000664.2:g.188992888G>A | GRCh38 |
| NC_000002.11:g.189857614G>A , CM000664.1:g.189857614G>A | GRCh37 |
| NC_000002.10:g.189565859G>A | NCBI36 |
| NG_007404.1:g.23516G>A , LRG_3:g.23516G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.998G>A | ENSP00000415346.2:p.Gly333Asp | |
| ENST00000304636.9:c.998G>A MANE Select | ENSP00000304408.4:p.Gly333Asp | |
| ENST00000304636.7:c.998G>A | ENSP00000304408.3:p.Gly333Asp | |
| ENST00000317840.9:c.998G>A | ENSP00000315243.6:p.Gly333Asp | |
| ENST00000450867.1:c.96G>A | ||
| NM_000090.3:c.998G>A , LRG_3t1:c.998G>A | NP_000081.1:p.Gly333Asp | |
| NM_000090.4:c.998G>A MANE Select | NP_000081.2:p.Gly333Asp |