Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.38796458G= , CM000675.2:g.38796458G= | GRCh38 |
| NC_000013.10:g.39370595G= , CM000675.1:g.39370595G= | GRCh37 |
| NC_000013.9:g.38268595G= | NCBI36 |
| NG_008125.2:g.114423G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207361.6:c.6019+11650G= MANE Select | NP_997244.4:n.6019+11650G= |
| ENST00000280481.9:c.6019+11650G= MANE Select | ENSP00000280481.7:n.6019+11650G= |
| NM_207361.5:c.6019+11650G= | NP_997244.4:n.6019+11650G= |
| ENST00000280481.8:c.6019+11650G= | ENSP00000280481.7:n.6019+11650G= |
| XM_011535057.1:c.6019+11650G= | XP_011533359.1:n.6019+11650G= |
| XR_941571.1:n.6327+11650G= | |
| XR_941571.2:n.6323+11650G= |