Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186073024G= , CM000666.2:g.186073024G= | GRCh38 |
| NC_000004.11:g.186994178G= , CM000666.1:g.186994178G= | GRCh37 |
| NC_000004.10:g.187231172G= | NCBI36 |
| NG_007278.1:g.8870G= , LRG_117:g.8870G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003265.3:c.-7-3589G= MANE Select | NP_003256.1:n.-7-3589G= |
| ENST00000296795.8:c.-7-3589G= MANE Select | ENSP00000296795.3:n.-7-3589G= |
| NM_003265.2:c.-7-3589G= , LRG_117t1:c.-7-3589G= | NP_003256.1:n.-7-3589G= |
| ENST00000296795.7:c.-7-3589G= | ENSP00000296795.2:n.-7-3589G= |
| ENST00000513189.1:c.-7-3589G= | ENSP00000423386.1:n.-7-3589G= |
| ENST00000698351.1:c.-7-3589G= | ENSP00000513674.1:n.-7-3589G= |
| ENST00000698352.1:c.-7-3589G= | ENSP00000513675.1:n.-7-3589G= |