Linked Data
ClinVar Variation Id:
1112055
ClinVar RCV Id:
RCV001438857
dbSNP Id:
rs2131529222
MyVariant Identifiers:
chr8:g.87588122A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86575894A>T , CM000670.2:g.86575894A>T | GRCh38 |
| NC_000008.10:g.87588122A>T , CM000670.1:g.87588122A>T | GRCh37 |
| NC_000008.9:g.87657238A>T | NCBI36 |
| NG_016980.1:g.172782T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2340T>A MANE Select | ENSP00000316605.5:p.Ser780= | |
| ENST00000681546.1:n.2160T>A | ||
| ENST00000681746.1:c.*751T>A | ENSP00000505959.1:n.*751T>A | |
| ENST00000320005.5:c.2340T>A | ENSP00000316605.5:p.Ser780= | |
| ENST00000517327.5:c.276+2795T>A | ENSP00000428329.1:n.276+2795T>A | |
| NM_019098.4:c.2340T>A | NP_061971.3:p.Ser780= | |
| XM_011517138.1:c.1926T>A | XP_011515440.1:p.Ser642= | |
| XM_011517138.2:c.1926T>A | XP_011515440.1:p.Ser642= | |
| NM_019098.5:c.2340T>A MANE Select | NP_061971.3:p.Ser780= |