Linked Data
MyVariant Identifiers:
chr11:g.118183550T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312835T>C , CM000673.2:g.118312835T>C | GRCh38 |
| NC_000011.9:g.118183550T>C , CM000673.1:g.118183550T>C | GRCh37 |
| NC_000011.8:g.117688760T>C | NCBI36 |
| NG_007383.1:g.13256T>C , LRG_38:g.13256T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.321T>C MANE Select | ENSP00000354566.4:p.Asp107= | |
| ENST00000361763.8:c.321T>C | ENSP00000354566.4:p.Asp107= | |
| ENST00000526146.5:n.867T>C | ||
| ENST00000528435.5:n.874T>C | ||
| ENST00000528600.1:c.303T>C | ENSP00000433975.1:p.Asp101= | |
| ENST00000529713.5:n.427T>C | ||
| ENST00000531913.1:n.692T>C | ||
| NM_000733.3:c.321T>C , LRG_38t1:c.321T>C | NP_000724.1:p.Asp107= | |
| NM_000733.4:c.321T>C MANE Select | NP_000724.1:p.Asp107= |