Linked Data
dbSNP Id:
rs2119537871
gnomAD v4:
10-99527816-G-A
MyVariant Identifiers:
chr10:g.101287573G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99527816G>A , CM000672.2:g.99527816G>A | GRCh38 |
| NC_000010.10:g.101287573G>A , CM000672.1:g.101287573G>A | GRCh37 |
| NC_000010.9:g.101277563G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_120618.1:n.567C>T |