Linked Data
MyVariant Identifiers:
chr8:g.87588113T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86575885T>G , CM000670.2:g.86575885T>G | GRCh38 |
| NC_000008.10:g.87588113T>G , CM000670.1:g.87588113T>G | GRCh37 |
| NC_000008.9:g.87657229T>G | NCBI36 |
| NG_016980.1:g.172791A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2349A>C MANE Select | ENSP00000316605.5:p.Ser783= | |
| ENST00000681546.1:n.2169A>C | ||
| ENST00000681746.1:c.*760A>C | ENSP00000505959.1:n.*760A>C | |
| ENST00000320005.5:c.2349A>C | ENSP00000316605.5:p.Ser783= | |
| ENST00000517327.5:c.276+2804A>C | ENSP00000428329.1:n.276+2804A>C | |
| NM_019098.4:c.2349A>C | NP_061971.3:p.Ser783= | |
| XM_011517138.1:c.1935A>C | XP_011515440.1:p.Ser645= | |
| XM_011517138.2:c.1935A>C | XP_011515440.1:p.Ser645= | |
| NM_019098.5:c.2349A>C MANE Select | NP_061971.3:p.Ser783= |