Linked Data
dbSNP Id:
rs12261589
gnomAD v2:
10-79540835-C-T
gnomAD v3:
10-77781077-C-T
gnomAD v4:
10-77781077-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.77781077C>T , CM000672.2:g.77781077C>T | GRCh38 |
| NC_000010.10:g.79540835C>T , CM000672.1:g.79540835C>T | GRCh37 |
| NC_000010.9:g.79210841C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000439688.1:n.800G>A |