Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104033922A= , CM000672.2:g.104033922A= | GRCh38 |
| NC_000010.10:g.105793680A= , CM000672.1:g.105793680A= | GRCh37 |
| NC_000010.9:g.105783670A= | NCBI36 |
| NG_007069.1:g.56959T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369733.8:c.3910+23T= | ENSP00000358748.3:n.3910+23T= | |
| ENST00000647647.1:c.186+23T= | ||
| ENST00000648076.2:c.4156+23T= MANE Select | ENSP00000497653.1:n.4156+23T= | |
| ENST00000353479.9:c.4156+23T= | ENSP00000340937.5:n.4156+23T= | |
| ENST00000369733.7:c.3910+23T= | ENSP00000358748.3:n.3910+23T= | |
| NM_000494.3:c.4156+23T= | NP_000485.3:n.4156+23T= | |
| NM_000494.4:c.4156+23T= MANE Select | NP_000485.3:n.4156+23T= |