Linked Data
MyVariant Identifiers:
chr11:g.116693479A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116822763A>T , CM000673.2:g.116822763A>T | GRCh38 |
| NC_000011.9:g.116693479A>T , CM000673.1:g.116693479A>T | GRCh37 |
| NC_000011.8:g.116198689A>T | NCBI36 |
| NG_012044.1:g.5533T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357780.5:c.72T>A MANE Select | ENSP00000350425.3:p.Ala24= | |
| ENST00000357780.4:c.72T>A | ENSP00000350425.3:p.Ala24= | |
| NM_000482.3:c.72T>A | NP_000473.2:p.Ala24= | |
| NM_000482.4:c.72T>A MANE Select | NP_000473.2:p.Ala24= |