Linked Data
ClinVar Variation Id:
1135863
ClinVar RCV Id:
RCV001471316
dbSNP Id:
rs1563711116
gnomAD v4:
8-86575834-A-T
MyVariant Identifiers:
chr8:g.87588062A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86575834A>T , CM000670.2:g.86575834A>T | GRCh38 |
| NC_000008.10:g.87588062A>T , CM000670.1:g.87588062A>T | GRCh37 |
| NC_000008.9:g.87657178A>T | NCBI36 |
| NG_016980.1:g.172842T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2400T>A MANE Select | ENSP00000316605.5:p.Thr800= | |
| ENST00000681546.1:n.2220T>A | ||
| ENST00000681746.1:c.*811T>A | ENSP00000505959.1:n.*811T>A | |
| ENST00000320005.5:c.2400T>A | ENSP00000316605.5:p.Thr800= | |
| ENST00000517327.5:c.276+2855T>A | ENSP00000428329.1:n.276+2855T>A | |
| NM_019098.4:c.2400T>A | NP_061971.3:p.Thr800= | |
| XM_011517138.1:c.1986T>A | XP_011515440.1:p.Thr662= | |
| XM_011517138.2:c.1986T>A | XP_011515440.1:p.Thr662= | |
| NM_019098.5:c.2400T>A MANE Select | NP_061971.3:p.Thr800= |