Linked Data
dbSNP Id:
rs1358940104
gnomAD v2:
12-122659724-T-TC
MyVariant Identifiers:
chr12:g.122659724_122659725insC (hg19)
chr12:g.122175177_122175178insC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.122175178dup , CM000674.2:g.122175178dup | GRCh38 |
| NC_000012.11:g.122659725dup , CM000674.1:g.122659725dup | GRCh37 |
| NC_000012.10:g.121225678dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000537729.5:c.-406+7396dup (LRRC43) | ENSP00000438751.1:n.-406+7396dup | |
| NM_152759.4:c.-406+7396dup (LRRC43) | NP_689972.3:n.-406+7396dup | |
| XM_011538326.1:c.-65-941dup (IL31) | XP_011536628.1:n.-65-941dup | |
| NM_152759.5:c.-406+7396dup (LRRC43) | NP_689972.3:n.-406+7396dup |