Canonical Allele Identifier: CA1067486265
Gene: IL21 HGNC NCBI

Linked Data

dbSNP Id: rs1799298387
gnomAD v3: 4-122613824-TGGA-T
gnomAD v4: 4-122613824-TGGA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613826_122613828del , CM000666.2:g.122613826_122613828del GRCh38
NC_000004.11:g.123534981_123534983del , CM000666.1:g.123534981_123534983del GRCh37
NC_000004.10:g.123754431_123754433del NCBI36
NG_031966.1:g.12231_12233del
NG_031966.2:g.12240_12242del

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.361-899_361-897del ENSP00000477555.1:n.361-899_361-897del
ENST00000647784.1:n.213-899_213-897del
ENST00000648588.1:c.361-899_361-897del MANE Select ENSP00000497915.1:n.361-899_361-897del
ENST00000264497.7:c.361-899_361-897del ENSP00000264497.3:n.361-899_361-897del
ENST00000611104.1:c.361-899_361-897del ENSP00000477555.1:n.361-899_361-897del
NM_001207006.2:c.361-899_361-897del NP_001193935.1:n.361-899_361-897del
NM_021803.3:c.361-899_361-897del NP_068575.1:n.361-899_361-897del
NM_021803.4:c.361-899_361-897del MANE Select NP_068575.1:n.361-899_361-897del
NM_001207006.3:c.361-899_361-897del NP_001193935.1:n.361-899_361-897del
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