Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.112831059G= , CM000664.2:g.112831059G= | GRCh38 |
| NC_000002.11:g.113588636G= , CM000664.1:g.113588636G= | GRCh37 |
| NC_000002.10:g.113305107G= | NCBI36 |
| NG_008851.1:g.10721C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263341.7:c.597+233C= MANE Select | ENSP00000263341.2:n.597+233C= | |
| ENST00000263341.6:c.597+233C= | ENSP00000263341.2:n.597+233C= | |
| ENST00000491056.5:n.1404+233C= | ||
| NM_000576.2:c.597+233C= | NP_000567.1:n.597+233C= | |
| XM_006712496.1:c.363+233C= | XP_006712559.1:n.363+233C= | |
| XM_017003988.2:c.504+233C= | XP_016859477.1:n.504+233C= | |
| NM_000576.3:c.597+233C= MANE Select | NP_000567.1:n.597+233C= |