Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31523827C= , CM000664.2:g.31523827C= | GRCh38 |
| NC_000002.11:g.31748897C= , CM000664.1:g.31748897C= | GRCh37 |
| NC_000002.10:g.31602401C= | NCBI36 |
| NG_008365.1:g.62145G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622030.2:c.*2369G= MANE Select | ENSP00000477587.1:n.*2369G= | |
| ENST00000622030.1:c.*2369G= | ENSP00000477587.1:n.*2369G= | |
| XM_011533069.1:c.*2369G= | XP_011531371.1:n.*2369G= | |
| XM_011533070.1:c.*2369G= | XP_011531372.1:n.*2369G= | |
| XM_011533071.1:c.*2369G= | XP_011531373.1:n.*2369G= | |
| XM_011533072.1:c.*2369G= | XP_011531374.1:n.*2369G= | |
| XM_011533069.2:c.*2369G= | XP_011531371.1:n.*2369G= | |
| XM_011533072.2:c.*2369G= | XP_011531374.1:n.*2369G= | |
| NM_000348.4:c.*2369G= MANE Select | NP_000339.2:n.*2369G= |