Canonical Allele Identifier: CA2671990982
Gene: IL21 HGNC NCBI
IL21-AS1 HGNC NCBI

Linked Data

gnomAD v4: 4-122619533-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122619533C>A , CM000666.2:g.122619533C>A GRCh38
NC_000004.11:g.123540688C>A , CM000666.1:g.123540688C>A GRCh37
NC_000004.10:g.123760138C>A NCBI36
NG_031966.1:g.6525G>T
NG_031966.2:g.6534G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.204+1168G>T (IL21) ENSP00000477555.1:n.204+1168G>T
ENST00000648588.1:c.204+1168G>T (IL21) MANE Select ENSP00000497915.1:n.204+1168G>T
ENST00000264497.7:c.204+1168G>T (IL21) ENSP00000264497.3:n.204+1168G>T
ENST00000611104.1:c.204+1168G>T (IL21) ENSP00000477555.1:n.204+1168G>T
NM_001207006.2:c.204+1168G>T (IL21) NP_001193935.1:n.204+1168G>T
NM_021803.3:c.204+1168G>T (IL21) NP_068575.1:n.204+1168G>T
NR_104126.1:n.510+41C>A (IL21-AS1)
NM_021803.4:c.204+1168G>T (IL21) MANE Select NP_068575.1:n.204+1168G>T
NM_001207006.3:c.204+1168G>T (IL21) NP_001193935.1:n.204+1168G>T
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