Linked Data
dbSNP Id:
rs34622242
MyVariant Identifiers:
chr12:g.122659875_122659876insT (hg19)
chr12:g.122175328_122175329insT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.122175328_122175329insT , CM000674.2:g.122175328_122175329insT | GRCh38 |
| NC_000012.11:g.122659875_122659876insT , CM000674.1:g.122659875_122659876insT | GRCh37 |
| NC_000012.10:g.121225828_121225829insT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000537729.5:c.-406+7546_-406+7547insT (LRRC43) | ENSP00000438751.1:n.-406+7546_-406+7547insT | |
| NM_152759.4:c.-406+7546_-406+7547insT (LRRC43) | NP_689972.3:n.-406+7546_-406+7547insT | |
| XM_011538326.1:c.-65-1092_-65-1091insA (IL31) | XP_011536628.1:n.-65-1092_-65-1091insA | |
| NM_152759.5:c.-406+7546_-406+7547insT (LRRC43) | NP_689972.3:n.-406+7546_-406+7547insT |