Linked Data
ClinVar Variation Id:
5038
ClinVar RCV Id:
RCV000005341
dbSNP Id:
rs119485095
COSMIC:
COSM5851567
PubMed:
PMID:19231187
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81354627G>A , CM000678.2:g.81354627G>A | GRCh38 |
| NC_000016.9:g.81388232G>A , CM000678.1:g.81388232G>A | GRCh37 |
| NC_000016.8:g.79945733G>A | NCBI36 |
| NG_009007.1:g.44662G>A , LRG_242:g.44662G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000648349.2:c.*213G>A | ENSP00000498114.1:n.*213G>A | |
| ENST00000648994.2:c.505G>A MANE Select | ENSP00000497351.1:p.Glu169Lys | |
| ENST00000650388.1:c.168-2158G>A | ENSP00000498081.1:n.168-2158G>A | |
| ENST00000674788.1:n.630G>A | ||
| ENST00000568107.2:c.505G>A | ENSP00000476795.1:p.Glu169Lys | |
| NM_022041.3:c.505G>A , LRG_242t1:c.505G>A | NP_071324.1:p.Glu169Lys | |
| XM_017023734.1:c.-135G>A | XP_016879223.1:n.-135G>A | |
| NM_001377486.1:c.-135G>A | NP_001364415.1:n.-135G>A | |
| NM_022041.4:c.505G>A MANE Select | NP_071324.1:p.Glu169Lys |