Linked Data
dbSNP Id:
rs2059991941
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.124346209T>A , CM000685.2:g.124346209T>A | GRCh38 |
| NC_000023.10:g.123480059T>A , CM000685.1:g.123480059T>A | GRCh37 |
| NC_000023.9:g.123307740T>A | NCBI36 |
| NG_007464.1:g.4910T>A , LRG_106:g.4910T>A | |
| NG_033796.2:g.390650T>A , LRG_782:g.390650T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698112.1:n.499-19552T>A (SH2D1A) | ||
| ENST00000698113.1:c.-434T>A (SH2D1A) | ENSP00000513571.1:n.-434T>A | |
| ENST00000469481.1:n.454-65613T>A (STAG2) | ||
| ENST00000635645.1:n.499-19552T>A (SH2D1A) |