Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.151181384C>G , CM000685.2:g.151181384C>G | GRCh38 |
| NC_000023.10:g.150349856C>G , CM000685.1:g.150349856C>G | GRCh37 |
| NC_000023.9:g.150100514C>G | NCBI36 |
| NG_016405.1:g.9801C>G | |
| NG_016405.2:g.9801C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218316.4:c.1801C>G MANE Select | ENSP00000218316.3:p.His601Asp | |
| ENST00000218316.3:c.1801C>G | ENSP00000218316.3:p.His601Asp | |
| ENST00000617907.1:c.1795C>G | ENSP00000484496.1:p.His599Asp | |
| NM_004224.3:c.1801C>G MANE Select | NP_004215.2:p.His601Asp | |
| XM_011531216.1:c.1060C>G | XP_011529518.1:p.His354Asp | |
| XM_011531216.2:c.1060C>G | XP_011529518.1:p.His354Asp |