Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.17084971T= , CM000684.2:g.17084971T= | GRCh38 |
| NC_000022.10:g.17565861T= , CM000684.1:g.17565861T= | GRCh37 |
| NC_000022.9:g.15945861T= | NCBI36 |
| NG_028257.1:g.5011T= , LRG_355:g.5011T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319363.10:c.-121T= | ENSP00000320936.6:n.-121T= | |
| ENST00000477874.1:n.18T= | ||
| ENST00000612619.1:c.-121T= | ENSP00000479970.1:n.-121T= | |
| NM_001289905.1:c.-121T= | NP_001276834.1:n.-121T= | |
| NM_014339.6:c.-121T= , LRG_355t1:c.-121T= | NP_055154.3:n.-121T= |