Linked Data
dbSNP Id:
rs1858631294
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625477C>G , CM000673.2:g.22625477C>G | GRCh38 |
| NC_000011.9:g.22647023C>G , CM000673.1:g.22647023C>G | GRCh37 |
| NC_000011.8:g.22603599C>G | NCBI36 |
| NG_007425.1:g.5365G>C , LRG_527:g.5365G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.334G>C MANE Select | ENSP00000330875.3:p.Val112Leu | |
| ENST00000327470.4:c.334G>C | ENSP00000330875.3:p.Val112Leu | |
| NM_022725.3:c.334G>C , LRG_527t1:c.334G>C | NP_073562.1:p.Val112Leu | |
| NM_022725.4:c.334G>C MANE Select | NP_073562.1:p.Val112Leu |