Linked Data
MyVariant Identifiers:
chr11:g.67353919T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586448T>A , CM000673.2:g.67586448T>A | GRCh38 |
| NC_000011.9:g.67353919T>A , CM000673.1:g.67353919T>A | GRCh37 |
| NC_000011.8:g.67110495T>A | NCBI36 |
| NG_012075.1:g.7854T>A , LRG_723:g.7854T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.396T>A | ENSP00000381604.1:p.Pro132= | |
| ENST00000398606.10:c.504T>A MANE Select | ENSP00000381607.3:p.Pro168= | |
| ENST00000646888.1:c.*220T>A | ENSP00000494477.1:n.*220T>A | |
| ENST00000398603.5:c.396T>A | ENSP00000381604.1:p.Pro132= | |
| ENST00000398606.7:c.504T>A | ENSP00000381607.3:p.Pro168= | |
| ENST00000467591.1:n.615T>A | ||
| ENST00000494593.1:n.1476T>A | ||
| ENST00000498765.5:c.567T>A | ||
| NM_000852.3:c.504T>A , LRG_723t1:c.504T>A | NP_000843.1:p.Pro168= | |
| NM_000852.4:c.504T>A MANE Select | NP_000843.1:p.Pro168= |