Linked Data
dbSNP Id:
rs6489188
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.122176229T>G , CM000674.2:g.122176229T>G | GRCh38 |
| NC_000012.11:g.122660776T>G , CM000674.1:g.122660776T>G | GRCh37 |
| NC_000012.10:g.121226729T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000537729.5:c.-405-8290T>G (LRRC43) | ENSP00000438751.1:n.-405-8290T>G | |
| NM_152759.4:c.-405-8290T>G (LRRC43) | NP_689972.3:n.-405-8290T>G | |
| XM_011538326.1:c.-65-1992A>C (IL31) | XP_011536628.1:n.-65-1992A>C | |
| NM_152759.5:c.-405-8290T>G (LRRC43) | NP_689972.3:n.-405-8290T>G |