HGVS | Genome Assembly |
---|---|
NC_000012.12:g.122175298T>A , CM000674.2:g.122175298T>A | GRCh38 |
NC_000012.11:g.122659845T>A , CM000674.1:g.122659845T>A | GRCh37 |
NC_000012.10:g.121225798T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000537729.5:c.-406+7516T>A (LRRC43) | ENSP00000438751.1:n.-406+7516T>A | |
NM_152759.4:c.-406+7516T>A (LRRC43) | NP_689972.3:n.-406+7516T>A | |
XM_011538326.1:c.-65-1061A>T (IL31) | XP_011536628.1:n.-65-1061A>T | |
NM_152759.5:c.-406+7516T>A (LRRC43) | NP_689972.3:n.-406+7516T>A |