Canonical Allele Identifier: CA1067486263
Gene: IL21 HGNC NCBI

Linked Data

dbSNP Id: rs983149807
gnomAD v3: 4-122613812-C-T
gnomAD v4: 4-122613812-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613812C>T , CM000666.2:g.122613812C>T GRCh38
NC_000004.11:g.123534967C>T , CM000666.1:g.123534967C>T GRCh37
NC_000004.10:g.123754417C>T NCBI36
NG_031966.1:g.12246G>A
NG_031966.2:g.12255G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.361-884G>A ENSP00000477555.1:n.361-884G>A
ENST00000647784.1:n.213-884G>A
ENST00000648588.1:c.361-884G>A MANE Select ENSP00000497915.1:n.361-884G>A
ENST00000264497.7:c.361-884G>A ENSP00000264497.3:n.361-884G>A
ENST00000611104.1:c.361-884G>A ENSP00000477555.1:n.361-884G>A
NM_001207006.2:c.361-884G>A NP_001193935.1:n.361-884G>A
NM_021803.3:c.361-884G>A NP_068575.1:n.361-884G>A
NM_021803.4:c.361-884G>A MANE Select NP_068575.1:n.361-884G>A
NM_001207006.3:c.361-884G>A NP_001193935.1:n.361-884G>A
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