Linked Data
dbSNP Id:
rs2112771452
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.118365803C>T , CM000667.2:g.118365803C>T | GRCh38 |
| NC_000005.9:g.117701498C>T , CM000667.1:g.117701498C>T | GRCh37 |
| NC_000005.8:g.117729397C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_104610.1:n.2658-14296G>A |