Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86632870G>C , CM000670.2:g.86632870G>C | GRCh38 |
| NC_000008.10:g.87645098G>C , CM000670.1:g.87645098G>C | GRCh37 |
| NC_000008.9:g.87714214G>C | NCBI36 |
| NG_016980.1:g.115806C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320005.6:c.1202C>G MANE Select | ENSP00000316605.5:p.Ala401Gly | |
| ENST00000681546.1:n.1022C>G | ||
| ENST00000681746.1:c.1202C>G | ENSP00000505959.1:p.Ala401Gly | |
| ENST00000320005.5:c.1202C>G | ENSP00000316605.5:p.Ala401Gly | |
| NM_019098.4:c.1202C>G | NP_061971.3:p.Ala401Gly | |
| XM_011517138.1:c.788C>G | XP_011515440.1:p.Ala263Gly | |
| XM_011517138.2:c.788C>G | XP_011515440.1:p.Ala263Gly | |
| NM_019098.5:c.1202C>G MANE Select | NP_061971.3:p.Ala401Gly |