Linked Data
ClinVar Variation Id:
56006
ClinVar RCV Id:
RCV000049415
dbSNP Id:
rs386833487
PubMed:
PMID:21394828
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107789649A>C , CM000669.2:g.107789649A>C | GRCh38 |
| NC_000007.13:g.107430094A>C , CM000669.1:g.107430094A>C | GRCh37 |
| NC_000007.12:g.107217330A>C | NCBI36 |
| NG_008046.1:g.18585T>G , LRG_683:g.18585T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340010.10:c.610T>G MANE Select | ENSP00000345873.5:p.Tyr204Asp | |
| ENST00000340010.9:c.610T>G | ENSP00000345873.5:p.Tyr204Asp | |
| ENST00000379083.7:c.*401T>G | ENSP00000368375.3:n.*401T>G | |
| NM_000111.2:c.610T>G , LRG_683t1:c.610T>G | NP_000102.1:p.Tyr204Asp | |
| XM_011515867.1:c.610T>G | XP_011514169.1:p.Tyr204Asp | |
| NM_000111.3:c.610T>G MANE Select | NP_000102.1:p.Tyr204Asp |