Linked Data
gnomAD v4:
X-124346321-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.124346321G>T , CM000685.2:g.124346321G>T | GRCh38 |
| NC_000023.10:g.123480171G>T , CM000685.1:g.123480171G>T | GRCh37 |
| NC_000023.9:g.123307852G>T | NCBI36 |
| NG_007464.1:g.5022G>T , LRG_106:g.5022G>T | |
| NG_033796.2:g.390762G>T , LRG_782:g.390762G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698112.1:n.499-19440G>T (SH2D1A) | ||
| ENST00000698113.1:c.-322G>T (SH2D1A) | ENSP00000513571.1:n.-322G>T | |
| ENST00000469481.1:n.454-65501G>T (STAG2) | ||
| ENST00000635645.1:n.499-19440G>T (SH2D1A) | ||
| NM_001114937.2:c.-322G>T (SH2D1A) | NP_001108409.1:n.-322G>T | |
| NM_002351.4:c.-322G>T , LRG_106t1:c.-322G>T (SH2D1A) | NP_002342.1:n.-322G>T |