Linked Data
dbSNP Id:
rs2137120021
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.84458199C>G , CM000675.2:g.84458199C>G | GRCh38 |
| NC_000013.10:g.85032334C>G , CM000675.1:g.85032334C>G | GRCh37 |
| NC_000013.9:g.83930335C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_046871.1:n.139-104165C>G | ||
| XR_942133.1:n.369-46280G>C | ||
| XR_942134.1:n.366-46280G>C |