Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104034328T= , CM000672.2:g.104034328T= | GRCh38 |
| NC_000010.10:g.105794086T= , CM000672.1:g.105794086T= | GRCh37 |
| NC_000010.9:g.105784076T= | NCBI36 |
| NG_007069.1:g.56553A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369733.8:c.3527A= | ENSP00000358748.3:p.Asp1176= | |
| ENST00000648076.2:c.3773A= MANE Select | ENSP00000497653.1:p.Asp1258= | |
| ENST00000353479.9:c.3773A= | ENSP00000340937.5:p.Asp1258= | |
| ENST00000369733.7:c.3527A= | ENSP00000358748.3:p.Asp1176= | |
| NM_000494.3:c.3773A= | NP_000485.3:p.Asp1258= | |
| NM_000494.4:c.3773A= MANE Select | NP_000485.3:p.Asp1258= |