Linked Data
dbSNP Id:
rs1312156913
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.114674809C>G , CM000674.2:g.114674809C>G | GRCh38 |
| NC_000012.11:g.115112614C>G , CM000674.1:g.115112614C>G | GRCh37 |
| NC_000012.10:g.113596997C>G | NCBI36 |
| NG_008315.1:g.14356G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349155.7:c.1066G>C MANE Select | ENSP00000257567.2:p.Asp356His | |
| ENST00000257566.7:c.1126G>C | ENSP00000257566.3:p.Asp376His | |
| ENST00000349155.6:c.1066G>C | ENSP00000257567.2:p.Asp356His | |
| ENST00000613550.1:c.1066G>C | ENSP00000480048.1:p.Asp356His | |
| NM_005996.3:c.1066G>C | NP_005987.3:p.Asp356His | |
| NM_016569.3:c.1126G>C | NP_057653.3:p.Asp376His | |
| NM_005996.4:c.1066G>C MANE Select | NP_005987.3:p.Asp356His | |
| NM_016569.4:c.1126G>C | NP_057653.3:p.Asp376His |