Canonical Allele Identifier: CA1490361252
Gene: IL21 HGNC NCBI

Linked Data

dbSNP Id: rs1471544704
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613889G>C , CM000666.2:g.122613889G>C GRCh38
NC_000004.11:g.123535044G>C , CM000666.1:g.123535044G>C GRCh37
NC_000004.10:g.123754494G>C NCBI36
NG_031966.1:g.12169C>G
NG_031966.2:g.12178C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.361-961C>G ENSP00000477555.1:n.361-961C>G
ENST00000647784.1:n.213-961C>G
ENST00000648588.1:c.361-961C>G MANE Select ENSP00000497915.1:n.361-961C>G
ENST00000264497.7:c.361-961C>G ENSP00000264497.3:n.361-961C>G
ENST00000611104.1:c.361-961C>G ENSP00000477555.1:n.361-961C>G
NM_001207006.2:c.361-961C>G NP_001193935.1:n.361-961C>G
NM_021803.3:c.361-961C>G NP_068575.1:n.361-961C>G
NM_021803.4:c.361-961C>G MANE Select NP_068575.1:n.361-961C>G
NM_001207006.3:c.361-961C>G NP_001193935.1:n.361-961C>G
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