Linked Data
MyVariant Identifiers:
chr11:g.118183388T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312673T>C , CM000673.2:g.118312673T>C | GRCh38 |
| NC_000011.9:g.118183388T>C , CM000673.1:g.118183388T>C | GRCh37 |
| NC_000011.8:g.117688598T>C | NCBI36 |
| NG_007383.1:g.13094T>C , LRG_38:g.13094T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.159T>C MANE Select | ENSP00000354566.4:p.Pro53= | |
| ENST00000361763.8:c.159T>C | ENSP00000354566.4:p.Pro53= | |
| ENST00000526146.5:n.705T>C | ||
| ENST00000528435.5:n.712T>C | ||
| ENST00000528600.1:c.141T>C | ENSP00000433975.1:p.Pro47= | |
| ENST00000529713.5:n.265T>C | ||
| ENST00000531913.1:n.530T>C | ||
| NM_000733.3:c.159T>C , LRG_38t1:c.159T>C | NP_000724.1:p.Pro53= | |
| NM_000733.4:c.159T>C MANE Select | NP_000724.1:p.Pro53= |