Linked Data
ClinVar Variation Id:
1111407
ClinVar RCV Id:
RCV001437959
dbSNP Id:
rs945309818
gnomAD v4:
8-86575852-G-T
MyVariant Identifiers:
chr8:g.87588080G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86575852G>T , CM000670.2:g.86575852G>T | GRCh38 |
| NC_000008.10:g.87588080G>T , CM000670.1:g.87588080G>T | GRCh37 |
| NC_000008.9:g.87657196G>T | NCBI36 |
| NG_016980.1:g.172824C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2382C>A MANE Select | ENSP00000316605.5:p.Gly794= | |
| ENST00000681546.1:n.2202C>A | ||
| ENST00000681746.1:c.*793C>A | ENSP00000505959.1:n.*793C>A | |
| ENST00000320005.5:c.2382C>A | ENSP00000316605.5:p.Gly794= | |
| ENST00000517327.5:c.276+2837C>A | ENSP00000428329.1:n.276+2837C>A | |
| NM_019098.4:c.2382C>A | NP_061971.3:p.Gly794= | |
| XM_011517138.1:c.1968C>A | XP_011515440.1:p.Gly656= | |
| XM_011517138.2:c.1968C>A | XP_011515440.1:p.Gly656= | |
| NM_019098.5:c.2382C>A MANE Select | NP_061971.3:p.Gly794= |