Canonical Allele Identifier: CA786427782

Gene: IL21

Linked Data

• dbSNP Id: rs1391364472
• gnomAD v3: 4-122613865-A-C
• gnomAD v4: 4-122613865-A-C
• MyVariant Identifiers: chr4:g.123535020A>C (hg19) ; chr4:g.122613865A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122613865A>C , CM000666.2:g.122613865A>C	GRCh38
NC_000004.11:g.123535020A>C , CM000666.1:g.123535020A>C	GRCh37
NC_000004.10:g.123754470A>C	NCBI36
NG_031966.1:g.12193T>G
NG_031966.2:g.12202T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000611104.2:c.361-937T>G	ENSP00000477555.1:n.361-937T>G
ENST00000647784.1:n.213-937T>G
ENST00000648588.1:c.361-937T>G MANE Select	ENSP00000497915.1:n.361-937T>G
ENST00000264497.7:c.361-937T>G	ENSP00000264497.3:n.361-937T>G
ENST00000611104.1:c.361-937T>G	ENSP00000477555.1:n.361-937T>G
NM_001207006.2:c.361-937T>G	NP_001193935.1:n.361-937T>G
NM_021803.3:c.361-937T>G	NP_068575.1:n.361-937T>G
NM_021803.4:c.361-937T>G MANE Select	NP_068575.1:n.361-937T>G
NM_001207006.3:c.361-937T>G	NP_001193935.1:n.361-937T>G