Linked Data
gnomAD v4:
X-124346259-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.124346259G>C , CM000685.2:g.124346259G>C | GRCh38 |
| NC_000023.10:g.123480109G>C , CM000685.1:g.123480109G>C | GRCh37 |
| NC_000023.9:g.123307790G>C | NCBI36 |
| NG_007464.1:g.4960G>C , LRG_106:g.4960G>C | |
| NG_033796.2:g.390700G>C , LRG_782:g.390700G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698112.1:n.499-19502G>C (SH2D1A) | ||
| ENST00000698113.1:c.-384G>C (SH2D1A) | ENSP00000513571.1:n.-384G>C | |
| ENST00000469481.1:n.454-65563G>C (STAG2) | ||
| ENST00000635645.1:n.499-19502G>C (SH2D1A) |