Linked Data
dbSNP Id:
rs2119652999
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1999215C>G , CM000673.2:g.1999215C>G | GRCh38 |
| NC_000011.9:g.2020445C>G , CM000673.1:g.2020445C>G | GRCh37 |
| NC_000011.8:g.1977021C>G | NCBI36 |
| NG_016165.1:g.3621G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_131224.1:n.249+2003G>C (H19) | ||
| XM_011520273.1:c.498-12326C>G (MRPL23) | XP_011518575.1:n.498-12326C>G | |
| XM_011520274.1:c.492-12326C>G (MRPL23) | XP_011518576.1:n.492-12326C>G | |
| XM_011520275.1:c.498-12326C>G (MRPL23) | XP_011518577.1:n.498-12326C>G | |
| XM_011520275.2:c.498-12326C>G (MRPL23) | XP_011518577.1:n.498-12326C>G | |
| NM_001400176.1:c.498-12326C>G (MRPL23) | NP_001387105.1:n.498-12326C>G |