Linked Data
dbSNP Id:
rs11241130
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111623085G>C , CM000667.2:g.111623085G>C | GRCh38 |
| NC_000005.9:g.110958782G>C , CM000667.1:g.110958782G>C | GRCh37 |
| NC_000005.8:g.110986681G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_040093.1:n.284-46334G>C |