Linked Data
MyVariant Identifiers:
chr11:g.116703498C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116832782C>A , CM000673.2:g.116832782C>A | GRCh38 |
| NC_000011.9:g.116703498C>A , CM000673.1:g.116703498C>A | GRCh37 |
| NC_000011.8:g.116208708C>A | NCBI36 |
| NG_008949.1:g.7875C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227667.8:c.198C>A MANE Select | ENSP00000227667.2:p.Gly66= | |
| ENST00000227667.7:c.198C>A | ENSP00000227667.2:p.Gly66= | |
| ENST00000375345.3:c.252C>A | ENSP00000364494.1:p.Gly84= | |
| ENST00000630701.1:c.252C>A | ENSP00000486182.1:p.Gly84= | |
| NM_000040.1:c.198C>A | NP_000031.1:p.Gly66= | |
| NM_000040.2:c.198C>A | NP_000031.1:p.Gly66= | |
| NM_000040.3:c.198C>A MANE Select | NP_000031.1:p.Gly66= |