Canonical Allele Identifier: CA1490361286
Gene: IL21 HGNC NCBI

Linked Data

dbSNP Id: rs1799300637
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613949C>G , CM000666.2:g.122613949C>G GRCh38
NC_000004.11:g.123535104C>G , CM000666.1:g.123535104C>G GRCh37
NC_000004.10:g.123754554C>G NCBI36
NG_031966.1:g.12109G>C
NG_031966.2:g.12118G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000611104.2:c.361-1021G>C ENSP00000477555.1:n.361-1021G>C
ENST00000647784.1:n.213-1021G>C
ENST00000648588.1:c.361-1021G>C MANE Select ENSP00000497915.1:n.361-1021G>C
ENST00000264497.7:c.361-1021G>C ENSP00000264497.3:n.361-1021G>C
ENST00000611104.1:c.361-1021G>C ENSP00000477555.1:n.361-1021G>C
NM_001207006.2:c.361-1021G>C NP_001193935.1:n.361-1021G>C
NM_021803.3:c.361-1021G>C NP_068575.1:n.361-1021G>C
NM_021803.4:c.361-1021G>C MANE Select NP_068575.1:n.361-1021G>C
NM_001207006.3:c.361-1021G>C NP_001193935.1:n.361-1021G>C
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