Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63038769G= , CM000670.2:g.63038769G= | GRCh38 |
| NC_000008.10:g.63951328G= , CM000670.1:g.63951328G= | GRCh37 |
| NC_000008.9:g.64113882G= | NCBI36 |
| NG_028126.1:g.5283C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260118.7:c.-1C= MANE Select | ENSP00000260118.6:n.-1C= | |
| ENST00000518113.2:c.-1C= | ENSP00000504520.1:n.-1C= | |
| ENST00000523788.2:n.27C= | ||
| ENST00000677327.1:n.639C= | ||
| ENST00000677459.1:c.-1C= | ENSP00000503731.1:n.-1C= | |
| ENST00000677482.1:c.-1C= | ENSP00000504590.1:n.-1C= | |
| ENST00000678069.1:n.34C= | ||
| ENST00000679326.1:c.-1C= | ENSP00000504262.1:n.-1C= | |
| ENST00000260118.6:c.-1C= | ENSP00000260118.6:n.-1C= | |
| ENST00000518966.5:n.33C= | ||
| ENST00000520609.5:n.33C= | ||
| ENST00000523788.1:n.34C= | ||
| NM_003878.2:c.-1C= | NP_003869.1:n.-1C= | |
| XM_011517623.1:c.-1C= | XP_011515925.1:n.-1C= | |
| XM_011517623.3:c.-1C= | XP_011515925.1:n.-1C= | |
| NM_003878.3:c.-1C= MANE Select | NP_003869.1:n.-1C= |