Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.62020027C= , CM000672.2:g.62020027C= | GRCh38 |
| NC_000010.10:g.63779786C= , CM000672.1:g.63779786C= | GRCh37 |
| NC_000010.9:g.63449792C= | NCBI36 |
| NG_030027.1:g.123774C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000279873.12:c.733+19706C= MANE Select | ENSP00000279873.7:n.733+19706C= | |
| ENST00000644638.1:c.734-4646C= | ENSP00000494412.1:n.734-4646C= | |
| ENST00000681100.1:c.733+19706C= | ENSP00000506119.1:n.733+19706C= | |
| ENST00000279873.11:c.733+19706C= | ENSP00000279873.7:n.733+19706C= | |
| NM_032199.2:c.733+19706C= | NP_115575.1:n.733+19706C= | |
| XM_011540262.1:c.503-30861C= | XP_011538564.1:n.503-30861C= | |
| XM_024448230.1:c.166+19706C= | XP_024303998.1:n.166+19706C= | |
| NM_032199.3:c.733+19706C= MANE Select | NP_115575.1:n.733+19706C= |