HGVS | Genome Assembly |
---|---|
NC_000012.12:g.122175180T>G , CM000674.2:g.122175180T>G | GRCh38 |
NC_000012.11:g.122659727T>G , CM000674.1:g.122659727T>G | GRCh37 |
NC_000012.10:g.121225680T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000537729.5:c.-406+7398T>G (LRRC43) | ENSP00000438751.1:n.-406+7398T>G | |
NM_152759.4:c.-406+7398T>G (LRRC43) | NP_689972.3:n.-406+7398T>G | |
XM_011538326.1:c.-65-943A>C (IL31) | XP_011536628.1:n.-65-943A>C | |
NM_152759.5:c.-406+7398T>G (LRRC43) | NP_689972.3:n.-406+7398T>G |