Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.77133469T= , CM000669.2:g.77133469T= | GRCh38 |
| NC_000007.13:g.76762786T= , CM000669.1:g.76762786T= | GRCh37 |
| NC_000007.12:g.76600722T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285871.5:c.-12+10737T= MANE Select | ENSP00000285871.4:n.-12+10737T= | |
| ENST00000285871.4:c.-12+10737T= | ENSP00000285871.4:n.-12+10737T= | |
| ENST00000415750.5:c.-12+11001T= | ENSP00000388649.1:n.-12+11001T= | |
| NM_020879.2:c.-12+10737T= | NP_065930.2:n.-12+10737T= | |
| XR_927691.1:n.48-4743A= | ||
| NM_020879.3:c.-12+10737T= MANE Select | NP_065930.2:n.-12+10737T= |