Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50910775C>T , CM000685.2:g.50910775C>T | GRCh38 |
| NC_000023.10:g.50653775C>T , CM000685.1:g.50653775C>T | GRCh37 |
| NC_000023.9:g.50670515C>T | NCBI36 |
| NG_012894.1:g.4992C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005448.2:c.-9C>T MANE Select | NP_005439.2:n.-9C>T |
| ENST00000252677.4:c.-9C>T MANE Select | ENSP00000252677.3:n.-9C>T |