Linked Data
ClinVar Variation Id:
39802
ClinVar RCV Id:
RCV000033023
dbSNP Id:
rs397514599
PubMed:
PMID:23084290
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.55656148T>C , CM000664.2:g.55656148T>C | GRCh38 |
| NC_000002.11:g.55883283T>C , CM000664.1:g.55883283T>C | GRCh37 |
| NC_000002.10:g.55736787T>C | NCBI36 |
| NG_033012.1:g.42763A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000447944.7:c.1424A>G MANE Select | ENSP00000400646.2:p.Glu475Gly | |
| ENST00000260604.8:c.*979A>G | ENSP00000260604.4:n.*979A>G | |
| ENST00000415374.5:c.1424A>G | ENSP00000393953.1:p.Glu475Gly | |
| ENST00000415489.1:c.431A>G | ||
| ENST00000447944.6:c.1424A>G | ENSP00000400646.2:p.Glu475Gly | |
| NM_033109.4:c.1424A>G | NP_149100.2:p.Glu475Gly | |
| XM_005264629.1:c.1184A>G | XP_005264686.1:p.Glu395Gly | |
| XM_011533142.1:c.1424A>G | XP_011531444.1:p.Glu475Gly | |
| XM_005264629.2:c.1184A>G | XP_005264686.1:p.Glu395Gly | |
| XM_017005172.1:c.1184A>G | XP_016860661.1:p.Glu395Gly | |
| XR_001739010.1:n.1454A>G | ||
| NM_033109.5:c.1424A>G MANE Select | NP_149100.2:p.Glu475Gly |