Canonical Allele Identifier: CA554478613
Gene: IL21 HGNC NCBI
IL21-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1252956143
gnomAD v2: 4-123540700-AAC-A
gnomAD v3: 4-122619545-AAC-A
gnomAD v4: 4-122619545-AAC-A
MyVariant Identifiers: chr4:g.123540701_123540702del (hg19) chr4:g.122619546_122619547del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122619546_122619547del , CM000666.2:g.122619546_122619547del GRCh38
NC_000004.11:g.123540701_123540702del , CM000666.1:g.123540701_123540702del GRCh37
NC_000004.10:g.123760151_123760152del NCBI36
NG_031966.1:g.6511_6512del
NG_031966.2:g.6520_6521del

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.204+1154_204+1155del (IL21) ENSP00000477555.1:n.204+1154_204+1155del
ENST00000648588.1:c.204+1154_204+1155del (IL21) MANE Select ENSP00000497915.1:n.204+1154_204+1155del
ENST00000264497.7:c.204+1154_204+1155del (IL21) ENSP00000264497.3:n.204+1154_204+1155del
ENST00000611104.1:c.204+1154_204+1155del (IL21) ENSP00000477555.1:n.204+1154_204+1155del
NM_001207006.2:c.204+1154_204+1155del (IL21) NP_001193935.1:n.204+1154_204+1155del
NM_021803.3:c.204+1154_204+1155del (IL21) NP_068575.1:n.204+1154_204+1155del
NR_104126.1:n.510+54_510+55del (IL21-AS1)
NM_021803.4:c.204+1154_204+1155del (IL21) MANE Select NP_068575.1:n.204+1154_204+1155del
NM_001207006.3:c.204+1154_204+1155del (IL21) NP_001193935.1:n.204+1154_204+1155del
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