Linked Data
ClinVar Variation Id:
1089991
ClinVar RCV Id:
RCV001408960
dbSNP Id:
rs2131529311
gnomAD v4:
8-86575927-T-C
MyVariant Identifiers:
chr8:g.87588155T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86575927T>C , CM000670.2:g.86575927T>C | GRCh38 |
| NC_000008.10:g.87588155T>C , CM000670.1:g.87588155T>C | GRCh37 |
| NC_000008.9:g.87657271T>C | NCBI36 |
| NG_016980.1:g.172749A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2307A>G MANE Select | ENSP00000316605.5:p.Ser769= | |
| ENST00000681546.1:n.2127A>G | ||
| ENST00000681746.1:c.*718A>G | ENSP00000505959.1:n.*718A>G | |
| ENST00000320005.5:c.2307A>G | ENSP00000316605.5:p.Ser769= | |
| ENST00000517327.5:c.276+2762A>G | ENSP00000428329.1:n.276+2762A>G | |
| NM_019098.4:c.2307A>G | NP_061971.3:p.Ser769= | |
| XM_011517138.1:c.1893A>G | XP_011515440.1:p.Ser631= | |
| XM_011517138.2:c.1893A>G | XP_011515440.1:p.Ser631= | |
| NM_019098.5:c.2307A>G MANE Select | NP_061971.3:p.Ser769= |