Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31531433T= , CM000664.2:g.31531433T= | GRCh38 |
| NC_000002.11:g.31756503T= , CM000664.1:g.31756503T= | GRCh37 |
| NC_000002.10:g.31610007T= | NCBI36 |
| NG_008365.1:g.54539A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622030.2:c.485A= MANE Select | ENSP00000477587.1:p.His162= | |
| ENST00000622030.1:c.485A= | ENSP00000477587.1:p.His162= | |
| NM_000348.3:c.485A= | NP_000339.2:p.His162= | |
| XM_011533069.1:c.263A= | XP_011531371.1:p.His88= | |
| XM_011533070.1:c.230A= | XP_011531372.1:p.His77= | |
| XM_011533071.1:c.230A= | XP_011531373.1:p.His77= | |
| XM_011533072.1:c.230A= | XP_011531374.1:p.His77= | |
| XM_011533069.2:c.263A= | XP_011531371.1:p.His88= | |
| XM_011533072.2:c.230A= | XP_011531374.1:p.His77= | |
| NM_000348.4:c.485A= MANE Select | NP_000339.2:p.His162= |