HGVS | Genome Assembly |
---|---|
NC_000012.12:g.122175329A>C , CM000674.2:g.122175329A>C | GRCh38 |
NC_000012.11:g.122659876A>C , CM000674.1:g.122659876A>C | GRCh37 |
NC_000012.10:g.121225829A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000537729.5:c.-406+7547A>C (LRRC43) | ENSP00000438751.1:n.-406+7547A>C | |
NM_152759.4:c.-406+7547A>C (LRRC43) | NP_689972.3:n.-406+7547A>C | |
XM_011538326.1:c.-65-1092T>G (IL31) | XP_011536628.1:n.-65-1092T>G | |
NM_152759.5:c.-406+7547A>C (LRRC43) | NP_689972.3:n.-406+7547A>C |