Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94401361G= , CM000669.2:g.94401361G= | GRCh38 |
| NC_000007.13:g.94030673G= , CM000669.1:g.94030673G= | GRCh37 |
| NC_000007.12:g.93868609G= | NCBI36 |
| NG_007405.1:g.11801G= , LRG_2:g.11801G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.226-206G= MANE Select | ENSP00000297268.6:n.226-206G= | |
| ENST00000297268.10:c.226-206G= | ENSP00000297268.6:n.226-206G= | |
| ENST00000620463.1:c.220-206G= | ENSP00000477719.1:n.220-206G= | |
| NM_000089.3:c.226-206G= , LRG_2t1:c.226-206G= | NP_000080.2:n.226-206G= | |
| NM_000089.4:c.226-206G= MANE Select | NP_000080.2:n.226-206G= |