Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47403075T= , CM000664.2:g.47403075T= | GRCh38 |
| NC_000002.11:g.47630214T= , CM000664.1:g.47630214T= | GRCh37 |
| NC_000002.10:g.47483718T= | NCBI36 |
| NG_007110.2:g.4952T= , LRG_218:g.4952T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000543555.6:c.-131T= | ENSP00000442697.1:n.-131T= | |
| ENST00000233146.6:c.-117T= | ENSP00000233146.2:n.-117T= | |
| ENST00000454849.5:c.-131T= | ENSP00000411482.1:n.-131T= | |
| ENST00000543555.5:c.-131T= | ENSP00000442697.1:n.-131T= | |
| NM_000251.2:c.-117T= , LRG_218t1:c.-117T= | NP_000242.1:n.-117T= | |
| NM_001258281.1:c.-131T= | NP_001245210.1:n.-131T= |