Linked Data
dbSNP Id:
rs2151762898
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.142392036C>T , CM000667.2:g.142392036C>T | GRCh38 |
| NC_000005.9:g.141771601C>T , CM000667.1:g.141771601C>T | GRCh37 |
| NC_000005.8:g.141751785C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_120664.1:n.506+38453C>T |