Linked Data
dbSNP Id:
rs1869974001
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.105714956T>A , CM000674.2:g.105714956T>A | GRCh38 |
| NC_000012.11:g.106108734T>A , CM000674.1:g.106108734T>A | GRCh37 |
| NC_000012.10:g.104632864T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_110108.1:n.54+10700T>A | ||
| NR_110109.1:n.55-206T>A | ||
| NR_110110.1:n.83+8100T>A | ||
| NR_110111.1:n.83+8100T>A | ||
| NR_110111.2:n.83+8100T>A |