Linked Data
ClinVar Variation Id:
10298
ClinVar RCV Id:
RCV000011011
dbSNP Id:
rs137852450
PubMed:
PMID:7728145
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154903968C>A , CM000685.2:g.154903968C>A | GRCh38 |
| NC_000023.10:g.154132243C>A , CM000685.1:g.154132243C>A | GRCh37 |
| NC_000023.9:g.153785437C>A | NCBI36 |
| NG_011403.1:g.123756G>T | |
| NG_011403.2:g.123756G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5936G>T MANE Select | ENSP00000353393.4:p.Gly1979Val | |
| ENST00000360256.8:c.5936G>T | ENSP00000353393.4:p.Gly1979Val | |
| NM_000132.3:c.5936G>T | NP_000123.1:p.Gly1979Val | |
| XM_011531126.1:c.5831G>T | XP_011529428.1:p.Gly1944Val | |
| NM_000132.4:c.5936G>T MANE Select | NP_000123.1:p.Gly1979Val |