Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149063024T= , CM000667.2:g.149063024T= | GRCh38 |
| NC_000005.9:g.148442587T= , CM000667.1:g.148442587T= | GRCh37 |
| NC_000005.8:g.148422780T= | NCBI36 |
| NG_007947.2:g.5151A= , LRG_269:g.5151A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515425.6:c.-2A= MANE Select | ENSP00000423660.1:n.-2A= | |
| ENST00000674983.1:c.-2A= | ENSP00000502387.1:n.-2A= | |
| ENST00000675793.1:c.-2A= | ENSP00000502039.1:n.-2A= | |
| ENST00000676056.1:c.-2A= | ENSP00000501827.1:n.-2A= | |
| ENST00000323829.9:c.-2A= | ENSP00000313025.5:n.-2A= | |
| ENST00000504091.1:n.35A= | ||
| ENST00000504690.5:c.-2A= | ENSP00000425627.1:n.-2A= | |
| ENST00000511307.5:c.-2A= | ENSP00000421420.1:n.-2A= | |
| ENST00000511949.5:n.39A= | ||
| ENST00000512049.5:c.-2A= | ENSP00000421860.1:n.-2A= | |
| ENST00000513604.5:c.-2A= | ENSP00000423111.1:n.-2A= | |
| ENST00000515425.5:c.-2A= | ENSP00000423660.1:n.-2A= | |
| NM_024577.3:c.-2A= , LRG_269t1:c.-2A= | NP_078853.2:n.-2A= | |
| NM_024577.4:c.-2A= MANE Select | NP_078853.2:n.-2A= |