Linked Data
MyVariant Identifiers:
chr11:g.116693377G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116822661G>T , CM000673.2:g.116822661G>T | GRCh38 |
| NC_000011.9:g.116693377G>T , CM000673.1:g.116693377G>T | GRCh37 |
| NC_000011.8:g.116198587G>T | NCBI36 |
| NG_012044.1:g.5635C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357780.5:c.174C>A MANE Select | ENSP00000350425.3:p.Leu58= | |
| ENST00000357780.4:c.174C>A | ENSP00000350425.3:p.Leu58= | |
| NM_000482.3:c.174C>A | NP_000473.2:p.Leu58= | |
| NM_000482.4:c.174C>A MANE Select | NP_000473.2:p.Leu58= |