Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86576027T= , CM000670.2:g.86576027T= | GRCh38 |
| NC_000008.10:g.87588255T= , CM000670.1:g.87588255T= | GRCh37 |
| NC_000008.9:g.87657371T= | NCBI36 |
| NG_016980.1:g.172649A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2207A= MANE Select | ENSP00000316605.5:p.Glu736= | |
| ENST00000681546.1:n.2027A= | ||
| ENST00000681746.1:c.*618A= | ENSP00000505959.1:n.*618A= | |
| ENST00000320005.5:c.2207A= | ENSP00000316605.5:p.Glu736= | |
| ENST00000517327.5:c.276+2662A= | ENSP00000428329.1:n.276+2662A= | |
| NM_019098.4:c.2207A= | NP_061971.3:p.Glu736= | |
| XM_011517138.1:c.1793A= | XP_011515440.1:p.Glu598= | |
| XM_011517138.2:c.1793A= | XP_011515440.1:p.Glu598= | |
| NM_019098.5:c.2207A= MANE Select | NP_061971.3:p.Glu736= |