Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.122175408C>T , CM000674.2:g.122175408C>T | GRCh38 |
| NC_000012.11:g.122659955C>T , CM000674.1:g.122659955C>T | GRCh37 |
| NC_000012.10:g.121225908C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000537729.5:c.-406+7626C>T (LRRC43) | ENSP00000438751.1:n.-406+7626C>T | |
| NM_152759.4:c.-406+7626C>T (LRRC43) | NP_689972.3:n.-406+7626C>T | |
| XM_011538326.1:c.-65-1171G>A (IL31) | XP_011536628.1:n.-65-1171G>A | |
| NM_152759.5:c.-406+7626C>T (LRRC43) | NP_689972.3:n.-406+7626C>T |