Linked Data
ClinVar Variation Id:
2826650
ClinVar RCV Id:
RCV003681409
MyVariant Identifiers:
chr8:g.87588146C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86575918C>T , CM000670.2:g.86575918C>T | GRCh38 |
| NC_000008.10:g.87588146C>T , CM000670.1:g.87588146C>T | GRCh37 |
| NC_000008.9:g.87657262C>T | NCBI36 |
| NG_016980.1:g.172758G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2316G>A MANE Select | ENSP00000316605.5:p.Arg772= | |
| ENST00000681546.1:n.2136G>A | ||
| ENST00000681746.1:c.*727G>A | ENSP00000505959.1:n.*727G>A | |
| ENST00000320005.5:c.2316G>A | ENSP00000316605.5:p.Arg772= | |
| ENST00000517327.5:c.276+2771G>A | ENSP00000428329.1:n.276+2771G>A | |
| NM_019098.4:c.2316G>A | NP_061971.3:p.Arg772= | |
| XM_011517138.1:c.1902G>A | XP_011515440.1:p.Arg634= | |
| XM_011517138.2:c.1902G>A | XP_011515440.1:p.Arg634= | |
| NM_019098.5:c.2316G>A MANE Select | NP_061971.3:p.Arg772= |