HGVS | Genome Assembly |
---|---|
NC_000012.12:g.122175226G>A , CM000674.2:g.122175226G>A | GRCh38 |
NC_000012.11:g.122659773G>A , CM000674.1:g.122659773G>A | GRCh37 |
NC_000012.10:g.121225726G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000537729.5:c.-406+7444G>A (LRRC43) | ENSP00000438751.1:n.-406+7444G>A | |
NM_152759.4:c.-406+7444G>A (LRRC43) | NP_689972.3:n.-406+7444G>A | |
XM_011538326.1:c.-65-989C>T (IL31) | XP_011536628.1:n.-65-989C>T | |
NM_152759.5:c.-406+7444G>A (LRRC43) | NP_689972.3:n.-406+7444G>A |