Linked Data
dbSNP Id:
rs10900020
gnomAD v2:
10-44827197-A-T
gnomAD v3:
10-44331749-A-T
gnomAD v4:
10-44331749-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44331749A>T , CM000672.2:g.44331749A>T | GRCh38 |
| NC_000010.10:g.44827197A>T , CM000672.1:g.44827197A>T | GRCh37 |
| NC_000010.9:g.44147203A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_945912.1:n.310+15799T>A | ||
| XR_001747171.1:n.332-33852T>A | ||
| XR_001747172.1:n.332-33852T>A | ||
| XR_001747173.1:n.332-33852T>A | ||
| XR_001747174.1:n.332-33852T>A |