Linked Data
MyVariant Identifiers:
chr11:g.67353958G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586487G>A , CM000673.2:g.67586487G>A | GRCh38 |
| NC_000011.9:g.67353958G>A , CM000673.1:g.67353958G>A | GRCh37 |
| NC_000011.8:g.67110534G>A | NCBI36 |
| NG_012075.1:g.7893G>A , LRG_723:g.7893G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.435G>A | ENSP00000381604.1:p.Val145= | |
| ENST00000398606.10:c.543G>A MANE Select | ENSP00000381607.3:p.Val181= | |
| ENST00000646888.1:c.*259G>A | ENSP00000494477.1:n.*259G>A | |
| ENST00000398603.5:c.435G>A | ENSP00000381604.1:p.Val145= | |
| ENST00000398606.7:c.543G>A | ENSP00000381607.3:p.Val181= | |
| ENST00000467591.1:n.654G>A | ||
| ENST00000494593.1:n.1515G>A | ||
| ENST00000498765.5:c.606G>A | ||
| NM_000852.3:c.543G>A , LRG_723t1:c.543G>A | NP_000843.1:p.Val181= | |
| NM_000852.4:c.543G>A MANE Select | NP_000843.1:p.Val181= |