Canonical Allele Identifier: CA105235721
Gene: IL21 HGNC NCBI

Linked Data

dbSNP Id: rs941666642
MyVariant Identifiers: chr4:g.123534981G>T (hg19) chr4:g.122613826G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613826G>T , CM000666.2:g.122613826G>T GRCh38
NC_000004.11:g.123534981G>T , CM000666.1:g.123534981G>T GRCh37
NC_000004.10:g.123754431G>T NCBI36
NG_031966.1:g.12232C>A
NG_031966.2:g.12241C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.361-898C>A ENSP00000477555.1:n.361-898C>A
ENST00000647784.1:n.213-898C>A
ENST00000648588.1:c.361-898C>A MANE Select ENSP00000497915.1:n.361-898C>A
ENST00000264497.7:c.361-898C>A ENSP00000264497.3:n.361-898C>A
ENST00000611104.1:c.361-898C>A ENSP00000477555.1:n.361-898C>A
NM_001207006.2:c.361-898C>A NP_001193935.1:n.361-898C>A
NM_021803.3:c.361-898C>A NP_068575.1:n.361-898C>A
NM_021803.4:c.361-898C>A MANE Select NP_068575.1:n.361-898C>A
NM_001207006.3:c.361-898C>A NP_001193935.1:n.361-898C>A
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