Linked Data
dbSNP Id:
rs2124859265
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.13854768C>G , CM000665.2:g.13854768C>G | GRCh38 |
| NC_000003.11:g.13896265C>G , CM000665.1:g.13896265C>G | GRCh37 |
| NC_000003.10:g.13871266C>G | NCBI36 |
| NG_008088.1:g.30354G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285018.5:c.334G>C MANE Select | ENSP00000285018.4:p.Ala112Pro | |
| ENST00000285018.4:c.334G>C | ENSP00000285018.4:p.Ala112Pro | |
| NM_004625.3:c.334G>C | NP_004616.2:p.Ala112Pro | |
| XM_011534090.1:c.133G>C | XP_011532392.1:p.Ala45Pro | |
| XM_011534091.1:c.133G>C | XP_011532393.1:p.Ala45Pro | |
| XM_011534091.2:c.133G>C | XP_011532393.1:p.Ala45Pro | |
| NM_004625.4:c.334G>C MANE Select | NP_004616.2:p.Ala112Pro |