Linked Data
dbSNP Id:
rs10484554
gnomAD v2:
6-31274555-C-T
gnomAD v3:
6-31306778-C-T
gnomAD v4:
6-31306778-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31306778C>T , CM000668.2:g.31306778C>T | GRCh38 |
| NC_000006.11:g.31274555C>T , CM000668.1:g.31274555C>T | GRCh37 |
| NC_000006.10:g.31382534C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_926691.1:n.949G>A | ||
| XR_926691.2:n.965G>A |