Canonical Allele Identifier: CA1490361255
Gene: IL21 HGNC NCBI

Linked Data

dbSNP Id: rs1578435484
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613896C>T , CM000666.2:g.122613896C>T GRCh38
NC_000004.11:g.123535051C>T , CM000666.1:g.123535051C>T GRCh37
NC_000004.10:g.123754501C>T NCBI36
NG_031966.1:g.12162G>A
NG_031966.2:g.12171G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000611104.2:c.361-968G>A ENSP00000477555.1:n.361-968G>A
ENST00000647784.1:n.213-968G>A
ENST00000648588.1:c.361-968G>A MANE Select ENSP00000497915.1:n.361-968G>A
ENST00000264497.7:c.361-968G>A ENSP00000264497.3:n.361-968G>A
ENST00000611104.1:c.361-968G>A ENSP00000477555.1:n.361-968G>A
NM_001207006.2:c.361-968G>A NP_001193935.1:n.361-968G>A
NM_021803.3:c.361-968G>A NP_068575.1:n.361-968G>A
NM_021803.4:c.361-968G>A MANE Select NP_068575.1:n.361-968G>A
NM_001207006.3:c.361-968G>A NP_001193935.1:n.361-968G>A
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