Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.49995089G= , CM000679.2:g.49995089G= | GRCh38 |
| NC_000017.10:g.48072453G= , CM000679.1:g.48072453G= | GRCh37 |
| NC_000017.9:g.45427452G= | NCBI36 |
| NG_023063.1:g.5136C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000434704.2:c.-91C= MANE Select | ENSP00000389870.2:n.-91C= | |
| NM_005220.2:c.-91C= | NP_005211.1:n.-91C= | |
| XM_011524458.1:c.-91C= | XP_011522760.1:n.-91C= | |
| NM_005220.3:c.-91C= MANE Select | NP_005211.1:n.-91C= |