Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136648177A= , CM000685.2:g.136648177A= | GRCh38 |
| NC_000023.10:g.135730336A= , CM000685.1:g.135730336A= | GRCh37 |
| NC_000023.9:g.135558002A= | NCBI36 |
| NG_007280.1:g.5001A= , LRG_141:g.5001A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.-72A= | ENSP00000512122.1:n.-72A= | |
| ENST00000695725.1:c.-72A= | ENSP00000512123.1:n.-72A= | |
| ENST00000370629.7:c.-72A= MANE Select | ENSP00000359663.2:n.-72A= | |
| NM_000074.2:c.-72A= , LRG_141t1:c.-72A= | NP_000065.1:n.-72A= | |
| NM_000074.3:c.-72A= MANE Select | NP_000065.1:n.-72A= |