Linked Data
dbSNP Id:
rs13143866
gnomAD v2:
4-123540758-G-A
gnomAD v3:
4-122619603-G-A
gnomAD v4:
4-122619603-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.122619603G>A , CM000666.2:g.122619603G>A | GRCh38 |
| NC_000004.11:g.123540758G>A , CM000666.1:g.123540758G>A | GRCh37 |
| NC_000004.10:g.123760208G>A | NCBI36 |
| NG_031966.1:g.6455C>T | |
| NG_031966.2:g.6464C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000611104.2:c.204+1098C>T (IL21) | ENSP00000477555.1:n.204+1098C>T | |
| ENST00000648588.1:c.204+1098C>T (IL21) MANE Select | ENSP00000497915.1:n.204+1098C>T | |
| ENST00000264497.7:c.204+1098C>T (IL21) | ENSP00000264497.3:n.204+1098C>T | |
| ENST00000611104.1:c.204+1098C>T (IL21) | ENSP00000477555.1:n.204+1098C>T | |
| NM_001207006.2:c.204+1098C>T (IL21) | NP_001193935.1:n.204+1098C>T | |
| NM_021803.3:c.204+1098C>T (IL21) | NP_068575.1:n.204+1098C>T | |
| NR_104126.1:n.510+111G>A (IL21-AS1) | ||
| NM_021803.4:c.204+1098C>T (IL21) MANE Select | NP_068575.1:n.204+1098C>T | |
| NM_001207006.3:c.204+1098C>T (IL21) | NP_001193935.1:n.204+1098C>T |