Canonical Allele Identifier: CA1490361235
Gene: IL21 HGNC NCBI

Linked Data

dbSNP Id: rs1329397874
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613841_122613843del , CM000666.2:g.122613841_122613843del GRCh38
NC_000004.11:g.123534996_123534998del , CM000666.1:g.123534996_123534998del GRCh37
NC_000004.10:g.123754446_123754448del NCBI36
NG_031966.1:g.12222_12224del
NG_031966.2:g.12231_12233del

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.361-908_361-906del ENSP00000477555.1:n.361-908_361-906del
ENST00000647784.1:n.213-908_213-906del
ENST00000648588.1:c.361-908_361-906del MANE Select ENSP00000497915.1:n.361-908_361-906del
ENST00000264497.7:c.361-908_361-906del ENSP00000264497.3:n.361-908_361-906del
ENST00000611104.1:c.361-908_361-906del ENSP00000477555.1:n.361-908_361-906del
NM_001207006.2:c.361-908_361-906del NP_001193935.1:n.361-908_361-906del
NM_021803.3:c.361-908_361-906del NP_068575.1:n.361-908_361-906del
NM_021803.4:c.361-908_361-906del MANE Select NP_068575.1:n.361-908_361-906del
NM_001207006.3:c.361-908_361-906del NP_001193935.1:n.361-908_361-906del
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