Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.122175266T= , CM000674.2:g.122175266T= | GRCh38 |
| NC_000012.11:g.122659813T= , CM000674.1:g.122659813T= | GRCh37 |
| NC_000012.10:g.121225766T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000537729.5:c.-406+7484T= (LRRC43) | ENSP00000438751.1:n.-406+7484T= | |
| NM_152759.4:c.-406+7484T= (LRRC43) | NP_689972.3:n.-406+7484T= | |
| XM_011538326.1:c.-65-1029A= (IL31) | XP_011536628.1:n.-65-1029A= | |
| NM_152759.5:c.-406+7484T= (LRRC43) | NP_689972.3:n.-406+7484T= |