Linked Data
MyVariant Identifiers:
chr11:g.55579614C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.55812138C>G , CM000673.2:g.55812138C>G | GRCh38 |
| NC_000011.9:g.55579614C>G , CM000673.1:g.55579614C>G | GRCh37 |
| NC_000011.8:g.55336190C>G | NCBI36 |
| NG_052620.1:g.5772C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000625203.2:c.672C>G MANE Select | ENSP00000485319.1:p.Thr224= | |
| ENST00000333973.3:c.672C>G | ENSP00000335529.2:p.Thr224= | |
| ENST00000623450.1:c.672C>G | ENSP00000485509.1:p.Thr224= | |
| ENST00000625203.1:c.672C>G | ENSP00000485319.1:p.Thr224= | |
| NM_001004738.1:c.672C>G | NP_001004738.1:p.Thr224= | |
| NM_001004738.2:c.672C>G MANE Select | NP_001004738.1:p.Thr224= |