Linked Data
ClinVar Variation Id:
97310
ClinVar RCV Id:
RCV000083556
dbSNP Id:
rs67330615
PubMed:
PMID:16786505
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38408915G>C , CM000685.2:g.38408915G>C | GRCh38 |
| NC_000023.10:g.38268168G>C , CM000685.1:g.38268168G>C | GRCh37 |
| NC_000023.9:g.38153112G>C | NCBI36 |
| NG_008471.1:g.61433G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000039007.5:c.757G>C MANE Select | ENSP00000039007.4:p.Ala253Pro | |
| ENST00000643344.1:c.*507G>C | ENSP00000496606.1:n.*507G>C | |
| ENST00000039007.4:c.757G>C | ENSP00000039007.4:p.Ala253Pro | |
| ENST00000465127.1:c.172-257206G>C | ENSP00000417050.1:n.172-257206G>C | |
| NM_000531.5:c.757G>C | NP_000522.3:p.Ala253Pro | |
| XM_017029556.1:c.757G>C | XP_016885045.1:p.Ala253Pro | |
| NM_000531.6:c.757G>C MANE Select | NP_000522.3:p.Ala253Pro |