Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31523859C= , CM000664.2:g.31523859C= | GRCh38 |
| NC_000002.11:g.31748929C= , CM000664.1:g.31748929C= | GRCh37 |
| NC_000002.10:g.31602433C= | NCBI36 |
| NG_008365.1:g.62113G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000622030.2:c.*2337G= MANE Select | ENSP00000477587.1:n.*2337G= | |
| ENST00000622030.1:c.*2337G= | ENSP00000477587.1:n.*2337G= | |
| XM_011533069.1:c.*2337G= | XP_011531371.1:n.*2337G= | |
| XM_011533070.1:c.*2337G= | XP_011531372.1:n.*2337G= | |
| XM_011533071.1:c.*2337G= | XP_011531373.1:n.*2337G= | |
| XM_011533072.1:c.*2337G= | XP_011531374.1:n.*2337G= | |
| XM_011533069.2:c.*2337G= | XP_011531371.1:n.*2337G= | |
| XM_011533072.2:c.*2337G= | XP_011531374.1:n.*2337G= | |
| NM_000348.4:c.*2337G= MANE Select | NP_000339.2:n.*2337G= |