Linked Data
MyVariant Identifiers:
chr8:g.87683275G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86671047G>C , CM000670.2:g.86671047G>C | GRCh38 |
| NC_000008.10:g.87683275G>C , CM000670.1:g.87683275G>C | GRCh37 |
| NC_000008.9:g.87752391G>C | NCBI36 |
| NG_016980.1:g.77629C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.390C>G MANE Select | ENSP00000316605.5:p.Ala130= | |
| ENST00000680314.1:n.151C>G | ||
| ENST00000681746.1:c.390C>G | ENSP00000505959.1:p.Ala130= | |
| ENST00000320005.5:c.390C>G | ENSP00000316605.5:p.Ala130= | |
| NM_019098.4:c.390C>G | NP_061971.3:p.Ala130= | |
| XM_011517138.1:c.-25C>G | XP_011515440.1:n.-25C>G | |
| XM_011517138.2:c.-25C>G | XP_011515440.1:n.-25C>G | |
| NM_019098.5:c.390C>G MANE Select | NP_061971.3:p.Ala130= |