Linked Data
dbSNP Id:
rs1867471399
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586543T>A , CM000673.2:g.67586543T>A | GRCh38 |
| NC_000011.9:g.67354014T>A , CM000673.1:g.67354014T>A | GRCh37 |
| NC_000011.8:g.67110590T>A | NCBI36 |
| NG_012075.1:g.7949T>A , LRG_723:g.7949T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.491T>A | ENSP00000381604.1:p.Val164Glu | |
| ENST00000398606.10:c.599T>A MANE Select | ENSP00000381607.3:p.Val200Glu | |
| ENST00000398603.5:c.491T>A | ENSP00000381604.1:p.Val164Glu | |
| ENST00000398606.7:c.599T>A | ENSP00000381607.3:p.Val200Glu | |
| ENST00000467591.1:n.710T>A | ||
| ENST00000494593.1:n.1571T>A | ||
| ENST00000498765.5:c.662T>A | ||
| NM_000852.3:c.599T>A , LRG_723t1:c.599T>A | NP_000843.1:p.Val200Glu | |
| NM_000852.4:c.599T>A MANE Select | NP_000843.1:p.Val200Glu |