Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40097355T= , CM000663.2:g.40097355T= | GRCh38 |
| NC_000001.10:g.40563027T= , CM000663.1:g.40563027T= | GRCh37 |
| NC_000001.9:g.40335614T= | NCBI36 |
| NG_009192.1:g.5116A= , LRG_690:g.5116A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000433473.7:c.-117A= | ENSP00000394863.3:n.-117A= | |
| NM_000310.3:c.-117A= , LRG_690t1:c.-117A= | NP_000301.1:n.-117A= | |
| NM_001142604.1:c.-117A= | NP_001136076.1:n.-117A= | |
| NM_001363695.1:c.-117A= | NP_001350624.1:n.-117A= |