Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.162272314T= , CM000664.2:g.162272314T= | GRCh38 |
| NC_000002.11:g.163128824T= , CM000664.1:g.163128824T= | GRCh37 |
| NC_000002.10:g.162837070T= | NCBI36 |
| NG_011495.1:g.51216A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022168.4:c.2528A= MANE Select | NP_071451.2:p.His843= |
| ENST00000649979.2:c.2528A= MANE Select | ENSP00000497271.1:p.His843= |
| NM_022168.3:c.2528A= | NP_071451.2:p.His843= |
| ENST00000263642.2:c.2528A= | ENSP00000263642.2:p.His843= |
| ENST00000648433.1:c.2411A= | ENSP00000496816.1:p.His804= |
| ENST00000649554.1:n.2138A= | |
| ENST00000679938.1:c.2216A= | ENSP00000505518.1:p.His739= |
| ENST00000697291.1:c.*2125A= | ENSP00000513228.1:n.*2125A= |
| XM_011511628.1:c.1811A= | XP_011509930.1:p.His604= |